Herbicidal Compositions Comprising Isoxazolo[5,4-B]Pyridines

ABSTRACT

Herbicidal compositions comprising isoxazolo[5,4-b]pyridines The present invention relates to herbicidal compositions comprising an isoxazolo[5,4-b]pyridine and at least one further compound selected from herbicidally active compounds and, if desired, safeners. The present invention also relates to the use of such a composition for controlling unwanted vegetation and to a method for controlling unwanted vegetation, which comprises allowing a composition to act on plants, their seeds and/or their habitat.

CROSS REFERENCE TO RELATED APPLICATIONS

This application is a divisional of U.S. application Ser. No.15/302,663, filed Oct. 7, 2016, the entire contents of which is herebyincorporated herein by reference. U.S. application Ser. No. 15/302,663is a National Stage Application of International Application No.PCT/EP2015/057613, filed Apr. 8, 2015, which claims the benefit of U.S.Provisional Application No. 61/977,663, filed Apr. 10, 2014, the entirecontents of each of which are hereby incorporated herein by reference.

The present invention relates to herbicidal compositions comprising anisoxazolo[5,4-b]pyridine and at least one further compound selected fromherbicidally active compounds and, if desired, safeners. The presentinvention also relates to the use of such a composition for controllingunwanted vegetation and to a method for controlling unwanted vegetation,which comprises allowing a composition to act on plants, their seedsand/or their habitat.

In the case of crop protection compositions, it is desirable inprinciple to increase the specific activity of an active compound andthe reliability of the effect. It is particularly desirable for the cropprotection composition to control the harmful plants effectively, but atthe same time to be compatible with the useful plants in question. Alsodesirable is a broad spectrum of activity allowing the simultaneouscontrol of a variety of harmful plants. Frequently, this cannot beachieved using a single herbicidally active compound.

With many highly effective herbicides, there is the problem that theircompatibility with useful plants, in particular dicotyledonous cropplants, such as cotton, oilseed rape and graminaceous plants, such asbarley, millet, corn, rice, wheat and sugar cane, is not alwayssatisfactory, i.e. in addition to the harmful plants, the crop plants,too, are damaged on a scale which cannot be tolerated. By reducing theapplication rates, the useful plants are spared; however, naturally, theextent of the control of harmful plants decreases too.

Frequently, it is a problem that herbicides can only be applied within anarrow time frame in order to achieve the desired herbicidal action,which time frame may be unpredictably influenced by weather conditions.

It is known that special combinations of different specifically activeherbicides may result in enhanced activity of an herbicide component inthe sense of a synergistic effect. In this manner, it may be feasible toreduce the application rates of herbicidally active compounds requiredfor controlling the harmful plants.

Furthermore, it is known that in some cases joint application ofspecifically acting herbicides with organic active compounds, some ofwhich may also have herbicidal activity, provides better crop plantcompatibility. In these cases, the active compounds act as antidotes orantagonists and are also referred to as safeners, since they reduce oreven prevent damage of herbicides to the crop plants.

Isoxazolo[5,4-b]pyridines of formula (I) and their agriculturally usefulsalts have been described for example in WO 2012010633 for use asherbicides.

US 2009163545 describes such compounds as lifespan-altering foreukaryotic organisms. According to WO 2009015208, particular ureaderivatives show an antibacterial effect. Potential routes for synthesisof isoxazolo[5,4-b]pyridine compounds are known from Elbannany et al,Pharmazie (1988) 43(2), 128-129 and Volochnyuk et al, Journal ofCombinatorial Chemistry (2010) 12(4), 510-517.

It is an object of the present invention to provide herbicidalcompositions which are highly active against unwanted harmful plants,showing enhanced activity in the sense of a synergistic effect. At thesame time, the compositions should have good compatibility with usefulplants. In addition, the compositions according to the invention shouldhave a broad spectrum of activity.

These and further objects are achieved by the herbicidal compositionsbelow.

Accordingly, the present invention relates to herbicidal compositionscomprising as component

A) an isoxazolo[5,4-b]pyridine compound of formula I

wherein the variables are as defined below:

R¹ is hydrogen, halogen, C₁-C₆-alkyl or C₁-C₆-haloalkyl;

R² is hydrogen, C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₁-C₆-hydroxyalkyl,C₃-C₆-cycloalkyl, C₃-C₆-halocycloalkyl, C₂-C₆-alkenyl or C₂-C₆-alkynyl;

R³ is hydrogen, halogen, hydroxy, C₁-C₆-alkyl, C₁-C₆-haloalkyl,C₁-C₆-hydroxyalkyl, C₁-C₆-alkoxy-C₁-C₆-alkyl,C₁-C₆-haloalkoxy-C₁-C₆-alkyl, C₃-C₆-cycloalkyl-C₁-C₆-alkyl,C₃-C₆-halocycloalkyl-C₁-C₆-alkyl, C₃-C₆-cycloalkyl,C₃-C₆-halocycloalkyl, C₁-C₄-alkyl-C₃-C₆-cycloalkyl, C₃-C₆-cycloalkenyl,C₃-C₆-halocycloalkenyl, phenyl-C₁-C₆-alkyl, heterocyclyl-C₁-C₆-alkyl,C₂-C₆-alkenyl, C₂-C₆-haloalkenyl, C₂-C₆-alkynyl, C₂-C₆-haloalkynyl,C₁-C₆-alkoxy, C₁-C₆-haloalkoxy, C₁-C₆-alkylthio, C₁-C₆-haloalkylthio,amino, C₁-C₆-alkylamino, N,N-di-(C₁-C₆)-alkylamino, heterocyclyl orphenyl; wherein heterocyclyl is a 5- or 6-membered saturated, partiallyunsaturated or aromatic monocyclic ring, which contains 1, 2, 3 or 4heteroatoms from the group consisting of O, N and S as ring members; andwherein the heterocyclyl and phenyl moieties of R³ can be unsubstitutedor substituted with one or more radicals selected from halogen, hydroxy,nitro, cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy-C₁-C₄-alkyl,C₃-C₆-cycloalkyl, C₂-C₆-alkenyl, C₂-C₆-alkynyl, C₁-C₄-alkoxy,C₁-C₄-haloalkoxy, C₁-C₄-alkoxycarbonyl, C₁-C₄-alkylthio,C₁-C₄-alkylsulfinyl, C₁-C₄-alkylsulfonyl, amino, C₁-C₄-alkylamino,N,N-di-(C₁-C₄)-alkylamino, heterocyclyl and phenyl; or itsagriculturally acceptable salt, carboxylic ester, thioester or amide;

and as component

B) at least one further herbicide (herbicide B) selected from theclasses b1) to b15):

b1) lipid biosynthesis inhibitors;

b2) acetolactate synthase inhibitors (ALS inhibitors);

b3) photosynthesis inhibitors;

b4) protoporphyrinogen-IX oxidase inhibitors,

b5) bleacher herbicides;

b6) enolpyruvyl shikimate 3-phosphate synthase inhibitors (EPSPinhibitors);

b7) glutamine synthetase inhibitors;

b8) 7,8-dihydropteroate synthase inhibitors (DHP inhibitors);

b9) mitosis inhibitors;

b10) inhibitors of the synthesis of very long chain fatty acids (VLCFAinhibitors);

b11) cellulose biosynthesis inhibitors;

b12) decoupler herbicides;

b13) auxinic herbicides;

b14) auxin transport inhibitors; and

b15) other herbicides selected from the group consisting of bromobutide,chlorflurenol, chlorflurenol-methyl,(1RS,2SR,4SR)-1,4-epoxy-p-menth-2-yl 2-methylbenzyl ether, cumyluron,dalapon, dazomet, difenzoquat, difenzoquat-metilsulfate, dimethipin,DSMA, dymron, endothal and its salts, etobenzanid, flamprop,flamprop-isopropyl, flamprop-methyl flamprop-M-isopropyl,flamprop-M-methyl, flurenol, flurenol-butyl, flurprimidol, fosamine,fosamine-ammonium, indanofan, maleic hydrazide, mefluidide, metam,methiozolin (CAS 403640-27-7), methyl azide, methyl bromide,methyl-dymron, methyl iodide, MSMA, oleic acid, oxaziclomefone,pelargonic acid, pyributicarb, quinoclamine, triaziflam, tridiphane and6-chloro-3-(2-cyclopropyl-6-methylphenoxy)-4-pyridazinol (CAS499223-49-3);

including their agriculturally acceptable salts or derivatives;

and as component C), if desired, safeners.

The compounds A of the formula (I) and their synthesis are known from WO2012/010633 A1.

The invention relates in particular to compositions in the form ofherbicidally active agrochemical compositions comprising a herbicidallyeffective amount of an active compound combination comprising at leastone isoxazolo[5,4-b]pyridine of formula (I) and at least one furtherherbicide selected from the herbicides B and, if desired, the safenersC, as defined above, and also at least one liquid and/or solid carrierand/or one or more surfactants and, if desired, one or more furtherauxiliaries customary for agrochemical compositions.

The invention also relates to compositions in the form of anagrochemical composition formulated as a 1-component compositioncomprising as component A an active compound combination comprising atleast one compound of formula (I) and, as component B), at least onefurther herbicide selected from the herbicides B, and, if desired, thesafeners C, and at least one solid or liquid carrier and/or one or moresurfactants and, if desired, one or more further auxiliaries customaryfor agrochemical compositions.

The invention also relates to compositions in the form of a agrochemicalcomposition formulated as a 2-component composition comprising a firstcomponent comprising as component A) at least oneisoxazolo[5,4-b]pyridine of formula (I), a solid or liquid carrierand/or one or more surfactants, and, as component B), at least onefurther herbicide selected from the herbicides B and, if desired,safeners C, a solid or liquid carrier and/or one or more surfactants,where additionally both components may also comprise further auxiliariescustomary for agrochemical compositions.

Surprisingly, the compositions according to the invention comprising ascomponent A) at least one isoxazolo[5,4-b]pyridine of formula (I) and,as component B), at least one herbicide B, have better herbicidalactivity, i.e. better activity against harmful plants, than would havebeen expected based on the herbicidal activity observed for theindividual compounds, or a broader activity spectrum. The herbicidalactivity to be expected for compositions based on the individualcompound can be calculated using Colby's formula (see below). If theactivity observed exceeds the expected additive activity of theindividual compounds, synergism is present.

Moreover, the time frame, within which the desired herbicidal action canbe achieved, may be expanded by the compositions according to theinvention comprising as component A) at least oneisoxazolo[5,4-b]pyridine of formula (I) and, as component B), at leastone herbicide B, and, if desired, a safener C. This allows a moreflexibly timed application of the compositions according to the presentinvention in comparison with the single compounds.

The invention furthermore relates to a method for controlling unwantedvegetation, in particular in fields where crop plants are cultivated.

The invention also relates to a method for the desiccation ordefoliation of plants.

As used herein, the terms “controlling” and “combating” are synonyms.

As used herein, the terms “undesirable vegetation” and “harmful plants”are synonyms.

If the isoxazolo[5,4-b]pyridine of formula (I), the herbicides B and/orthe safeners C as described herein are capable of forming geometricalisomers, for example E/Z isomers, it is possible to use both, the pureisomers and mixtures thereof, in the compositions according to theinvention.

If the isoxazolo[5,4-b]pyridine of formula (I), the herbicides B and/orthe safeners C as described herein have one or more centers of chiralityand, as a consequence, are present as enantiomers or diastereomers, itis possible to use both, the pure enantiomers and diastereomers andtheir mixtures, in the compositions according to the invention.

If the isoxazolo[5,4-b]pyridine of formula (I), the herbicides B and/orthe safeners C as described herein have ionizable functional groups,they can also be employed in the form of their agriculturally acceptablesalts. Suitable are, in general, the salts of those cations and the acidaddition salts of those acids whose cations and anions, respectively,have no adverse effect on the activity of the active compounds.

Preferred cations are the ions of the alkali metals, preferably oflithium, sodium and potassium, of the alkaline earth metals, preferablyof calcium and magnesium, and of the transition metals, preferably ofmanganese, copper, zinc and iron, further ammonium and substitutedammonium in which one to four hydrogen atoms are replaced byC₁-C₄-alkyl, hydroxy-C₁-C₄-alkyl, C₁-C₄-alkoxy-C₁-C₄-alkyl,hydroxy-C₁-C₄-alkoxy-C₁-C₄-alkyl, phenyl or benzyl, preferably ammonium,methylammonium, isopropylammonium, dimethylammonium,diisopropylammonium, trimethylammonium, heptylammonium, dodecylammonium,tetradecylammonium, tetramethylammonium, tetraethylammonium,tetrabutylammonium, 2-hydroxyethylammonium (olamine salt),2-(2-hydroxyeth-1-oxy)eth-1-ylammonium (diglycolamine salt),di(2-hydroxyeth-1-yl)ammonium (diolamine salt),tris(2-hydroxyethyl)ammonium (trolamine salt),tris(2-hydroxypropyl)ammonium, benzyltrimethylammonium,benzyltriethylammonium, N,N,N-trimethylethanolammonium (choline salt),furthermore phosphonium ions, sulfonium ions, preferablytri(C₁-C₄-alkyl)sulfonium, such as trimethylsulfonium, and sulfoxoniumions, preferably tri(C₁-C₄-alkyl)sulfoxonium, and finally the salts ofpolybasic amines such as N,N-bis-(3-aminopropyl)methylamine anddiethylenetriamine.

Anions of useful acid addition salts are primarily chloride, bromide,fluoride, iodide, hydrogensulfate, methylsulfate, sulfate,dihydrogenphosphate, hydrogenphosphate, nitrate, bicarbonate, carbonate,hexafluorosilicate, hexafluorophosphate, benzoate and also the anions ofC₁-C₄-alkanoic acids, preferably formate, acetate, propionate andbutyrate.

Isoxazolo[5,4-b]pyridines of formula (I), herbicides B and/or safeners Cas described herein having a carboxyl group can be employed in the formof the acid, in the form of an agriculturally suitable salt as mentionedabove or else in the form of an agriculturally acceptable derivative,for example as amides, as esters, and also as thioesters.

Further embodiments of the present invention are evident from theclaims, the description and the examples. It is to be understood thatthe features mentioned above and still to be illustrated below of thesubject matter of the invention can be applied not only in thecombination given in each particular case but also in othercombinations, without leaving the scope of the invention.

The terms used for organic groups in the definition of the variablesare, for example the expression “alkyl”, collective terms whichrepresent the individual members of these groups of organic units.

The prefix C_(x)-C_(y) denotes the number of possible carbon atoms inthe particular case.

halogen: fluorine, chlorine, bromine or iodine, especially fluorine,chlorine or bromine;

alkyl and the alkyl moieties of composite groups such as alkoxy,alkylamino, alkylthio, alkoxycarbonyl: saturated straight-chain orbranched hydrocarbon radicals having 1 to 10 carbon atoms, preferablyC₁-C₆-alkyl or C₁-C₄-alkyl, such as methyl, ethyl, propyl,1-methylethyl, butyl, 1-methylpropyl, 2-methylpropyl, 1,1-dimethylethyl,pentyl, 1-methylbutyl, 2-methylbutyl, 3-methylbutyl, 2,2-dimethylpropyl,1-ethylpropyl, hexyl, 1,1-dimethylpropyl, 1,2-dimethylpropyl,1-methylpentyl, 2-methylpentyl, 3-methylpentyl, 4-methylpentyl,1,1-dimethylbutyl, 1,2-dimethylbutyl, 1,3-dimethylbutyl,2,2-dimethylbutyl, 2,3-dimethylbutyl, 3,3-dimethylbutyl, 1-ethylbutyl,2-ethylbutyl, 1,1,2-trimethylpropyl, 1,2,2-trimethylpropyl,1-ethyl-1-methylpropyl and 1-ethyl-2-methylpropyl; heptyl, octyl,2-ethylhexyl and positional isomers thereof; nonyl, decyl and positionalisomers thereof;

haloalkyl: straight-chain or branched alkyl groups having 1 to 10 carbonatoms (as mentioned above), preferably C₁-C₆-haloalkyl orC₁-C₄-haloalkyl, where some or all of the hydrogen atoms in these groupsare replaced by halogen atoms as mentioned above. In one embodiment, thealkyl groups are substituted at least once or completely by a particularhalogen atom, preferably fluorine, chlorine or bromine. In a furtherembodiment, the alkyl groups are partially or fully halogenated bydifferent halogen atoms; in the case of mixed halogen substitutions, thecombination of chlorine and fluorine is preferred. Particular preferenceis given to (C₁-C₃)-haloalkyl, more preferably (C₁-C₂)-haloalkyl, suchas chloromethyl, bromomethyl, dichloromethyl, trichloromethyl,fluoromethyl, difluoromethyl, trifluoromethyl, chlorofluoromethyl,dichlorofluoromethyl, chlorodifluoromethyl, 1-chloroethyl, 1-bromoethyl,1-fluoroethyl, 2-fluoroethyl, 2,2-difluoroethyl, 2,2,2-trifluoroethyl,2-chloro-2-fluoroethyl, 2-chloro-2,2-difluoroethyl,2,2-dichloro-2-fluoroethyl, 2,2,2-trichloroethyl, pentafluoroethyl or1,1,1-trifluoroprop-2-yl;

alkenyl and also the alkenyl moieties in composite groups, such asalkenyloxy: unsaturated straight-chain or branched hydrocarbon radicalshaving 2 to 10 carbon atoms and one double bond in any position.According to the invention, it may be preferred to use small alkenylgroups, such as (C₂-C₆)-alkenyl; on the other hand, it may also bepreferred to employ larger alkenyl groups, such as (C₅-C₈)-alkenyl.Examples of C₂-C₆-alkenyl groups are: ethenyl, 1-propenyl, 2-propenyl,1-methylethenyl, 1-butenyl, 2-butenyl, 3-butenyl, 1-methyl-1-propenyl,2-methyl-1-propenyl, 1-methyl-2-propenyl, 2-methyl-2-propenyl,1-pentenyl, 2-pentenyl, 3-pentenyl, 4-pentenyl, 1-methyl-1-butenyl,2-methyl-1-butenyl, 3-methyl-1-butenyl, 1-methyl-2-butenyl,2-methyl-2-butenyl, 3-methyl-2-butenyl, 1-methyl-3-butenyl,2-methyl-3-butenyl, 3-methyl-3-butenyl, 1,1-dimethyl-2-propenyl,1,2-dimethyl-1-propenyl, 1,2-dimethyl-2-propenyl, 1-ethyl-1-propenyl,1-ethyl-2-propenyl, 1-hexenyl, 2-hexenyl, 3-hexenyl, 4-hexenyl,5-hexenyl, 1-methyl-1-pentenyl, 2-methyl-1-pentenyl,3-methyl-1-pentenyl, 4-methyl-1-pentenyl, 1-methyl-2-pentenyl,2-methyl-2-pentenyl, 3-methyl-2-pentenyl, 4-methyl-2-pentenyl,1-methyl-3-pentenyl, 2-methyl-3-pentenyl, 3-methyl-3-pentenyl,4-methyl-3-pentenyl, 1-methyl-4-pentenyl, 2-methyl-4-pentenyl,3-methyl-4-pentenyl, 4-methyl-4-pentenyl, 1,1-dimethyl-2-butenyl,1,1-dimethyl-3-butenyl, 1,2-dimethyl-1-butenyl, 1,2-dimethyl-2-butenyl,1,2-dimethyl-3-butenyl, 1,3-dimethyl-1-butenyl, 1,3-dimethyl-2-butenyl,1,3-dimethyl-3-butenyl, 2,2-dimethyl-3-butenyl, 2,3-dimethyl-1-butenyl,2,3-dimethyl-2-butenyl, 2,3-dimethyl-3-butenyl, 3,3-dimethyl-1-butenyl,3,3-dimethyl-2-butenyl, 1-ethyl-1-butenyl, 1-ethyl-2-butenyl,1-ethyl-3-butenyl, 2-ethyl-1-butenyl, 2-ethyl-2-butenyl,2-ethyl-3-butenyl, 1,1,2-trimethyl-2-propenyl,1-ethyl-1-methyl-2-propenyl, 1-ethyl-2-methyl-1-propenyl and1-ethyl-2-methyl-2-propenyl;

alkynyl and the alkynyl moieties in composite groups: straight-chain orbranched hydrocarbon groups having 2 to 10 carbon atoms and one triplebond in any position, for example C₂-C₆-alkynyl, such as ethynyl,1-propynyl, 2-propynyl, 1-butynyl, 2-butynyl, 3-butynyl,1-methyl-2-propynyl, 1-pentynyl, 2-pentynyl, 3-pentynyl, 4-pentynyl,1-methyl-2-butynyl, 1-methyl-3-butynyl, 2-methyl-3-butynyl,3-methyl-1-butynyl, 1,1-dimethyl-2-propynyl, 1-ethyl-2-propynyl,1-hexynyl, 2-hexynyl, 3-hexynyl, 4-hexynyl, 5-hexynyl,1-methyl-2-pentynyl, 1-methyl-3-pentynyl, 1-methyl-4-pentynyl,2-methyl-3-pentynyl, 2-methyl-4-pentynyl, 3-methyl-1-pentynyl,3-methyl-4-pentynyl, 4-methyl-1-pentynyl, 4-methyl-2-pentynyl,1,1-dimethyl-2-butynyl, 1,1-dimethyl-3-butynyl, 1,2-dimethyl-3-butynyl,2,2-dimethyl-3-butynyl, 3,3-dimethyl-1-butynyl, 1-ethyl-2-butynyl,1-ethyl-3-butynyl, 2-ethyl-3-butynyl and 1-ethyl-1-methyl-2-propynyl;

cycloalkyl and also the cycloalkyl moieties in composite groups: mono-or bicyclic saturated hydrocarbon groups having 3 to 10, in particular 3to 6, carbon ring members. Examples for C₃-C₆-cycloalkyl are:cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl orcyclooctyl. Examples of bicyclic radicals comprise bicyclo[2.2.1]heptyl,bicyclo[3.1.1]heptyl, bicyclo[2.2.2]octyl and bicyclo[3.2.1]octyl;

halocycloalkyl and the halocycloalkyl moieties in composite groups:monocyclic saturated hydrocarbon groups having 3 to 10 carbon ringmembers (as mentioned above) in which some or all of the hydrogen atomsmay be replaced by halogen atoms as mentioned above, in particularfluorine, chlorine and bromine;

cycloalkenyl: monocyclic monounsaturated hydrocarbon groups having 3 to10, 3 to 8, 3 to 6, preferably 5 to 6, carbon ring members, such ascyclopenten-1-yl, cyclopenten-3-yl, cyclohexen-1-yl, cyclohexen-3-yl,cyclohexen-4-yl and the like;

alkoxy: an alkyl group as defined above, which is attached via anoxygen, preferably having 1 to 10, more preferably 1 to 6 or 1 to 4carbon atoms. Examples are: methoxy, ethoxy, n-propoxy, 1-methylethoxy,butoxy, 1-methylpropoxy, 2-methylpropoxy or 1,1-dimethylethoxy, and alsofor example, pentoxy, 1-methylbutoxy, 2-methylbutoxy, 3-methylbutoxy,1,1-dimethylpropoxy, 1,2-dimethylpropoxy, 2,2-dimethylpropoxy,1-ethylpropoxy, hexoxy, 1-methylpentoxy, 2-methylpentoxy,3-methylpentoxy, 4-methylpentoxy, 1,1-dimethylbutoxy,1,2-dimethylbutoxy, 1,3-dimethylbutoxy, 2,2-dimethylbutoxy,2,3-dimethylbutoxy, 3,3-dimethylbutoxy, 1-ethylbutoxy, 2-ethylbutoxy,1,1,2-trimethylpropoxy, 1,2,2-trimethylpropoxy, 1-ethyl-1-methylpropoxyor 1-ethyl-2-methylpropoxy;

haloalkoxy: alkoxy as defined above, where some or all of the hydrogenatoms in these groups are replaced by halogen atoms as described aboveunder haloalkyl, in particular by fluorine, chlorine or bromine.Examples are OCH₂F, OCHF₂, OCF₃, OCH₂Cl, OCHCl₂, OCCl₃,chlorofluoromethoxy, dichlorofluoromethoxy, chlorodifluoromethoxy,2-fluoroethoxy, 2-chloroethoxy, 2-bromoethoxy, 2-iodoethoxy,2,2-difluoroethoxy, 2,2,2-trifluoroethoxy, 2-chloro-2-fluoroethoxy,2-chloro-2,2-difluoroethoxy, 2,2-dichloro-2-fluoroethoxy,2,2,2-trichloroethoxy, OC₂F₅, 2-fluoropropoxy, 3-fluoropropoxy,2,2-difluoropropoxy, 2,3-difluoropropoxy, 2-chloropropoxy,3-chloropropoxy, 2,3-dichloropropoxy, 2-bromopropoxy, 3-bromopropoxy,3,3,3-trifluoropropoxy, 3,3,3-trichloropropoxy, OCH₂-C₂F₅, OCF₂—C₂F₅,1-(CH₂F)-2-fluoroethoxy, 1-(CH₂Cl)-2-chloroethoxy,1-(CH₂Br)-2-bromoethoxy, 4-fluorobutoxy, 4-chlorobutoxy, 4-bromobutoxyor nonafluorobutoxy; and also 5-fluoropentoxy, 5-chloropentoxy,5-bromopentoxy, 5-iodopentoxy, undecafluoropentoxy, 6-fluorohexoxy,6-chlorohexoxy, 6-bromohexoxy, 6-iodohexoxy or dodecafluorohexoxy;

aryl: 6 to 10-membered, aromatic carbocycle with 6, 7, 8, 9 or 10 carbonatoms. Examples of preferred aryl are phenyl or naphthyl;

heterocyclyl: 5- or 6-membered saturated, partially unsaturated oraromatic monocyclic ring system, which contains 1, 2, 3 or 4 heteroatomsfrom the group consisting of O, N and S as ring members, where theheterocycle in question may be attached via a carbon atom or, ifpresent, via a nitrogen atom. In particular:

a five- or six-membered saturated or partially unsaturated heterocyclewhich comprises one, two, three or four heteroatoms from the groupconsisting of O, N and S as ring members: for example monocyclicsaturated or partially unsaturated heterocycles which, in addition tocarbon ring members, comprise one, two or three nitrogen atoms and/orone oxygen or sulfur atom or one or two oxygen and/or sulfur atoms, forexample aziridine, oxirane, 2-tetrahydrofuranyl, 3-tetrahydrofuranyl,2-tetrahydrothienyl, 3-tetrahydrothienyl, 2-pyrrolidinyl,3-pyrrolidinyl, 3-isoxazolidinyl, 4-isoxazolidinyl, 5-isoxazolidinyl,3-isothiazolidinyl, 4-isothiazolidinyl, 5-isothiazolidinyl,3-pyrazolidinyl, 4-pyrazolidinyl, 5-pyrazolidinyl, 2-oxazolidinyl,4-oxazolidinyl, 5-oxazolidinyl, 2-thiazolidinyl, 4-thiazolidinyl,5-thiazolidinyl, 2-imidazolidinyl, 4-imidazolidinyl,1,2,4-oxadiazolidin-3-yl, 1,2,4-oxadiazolidin-5-yl,1,2,4-thiadiazolidin-3-yl, 1,2,4-thiadiazolidin-5-yl,1,2,4-triazolidin-3-yl, 1,3,4-oxadiazolidin-2-yl,1,3,4-thiadiazolidin-2-yl, 1,3,4-triazolidin-2-yl, 2,3-dihydrofur-2-yl,2,3-dihydrofur-3-yl, 2,4-dihydrofur-2-yl, 2,4-dihydrofur-3-yl,2,3-dihydrothien-2-yl, 2,3-dihydrothien-3-yl, 2,4-dihydrothien-2-yl,2,4-dihydrothien-3-yl, 2-pyrrolin-2-yl, 2-pyrrolin-3-yl,3-pyrrolin-2-yl, 3-pyrrolin-3-yl, 2-isoxazolin-3-yl, 3-isoxazolin-3-yl,4-isoxazolin-3-yl, 2-isoxazolin-4-yl, 3-isoxazolin-4-yl,4-isoxazolin-4-yl, 2-isoxazolin-5-yl, 3-isoxazolin-5-yl,4-isoxazolin-5-yl, 2-isothiazolin-3-yl, 3-isothiazolin-3-yl,4-isothiazolin-3-yl, 2-isothiazolin-4-yl, 3-isothiazolin-4-yl,4-isothiazolin-4-yl, 2-isothiazolin-5-yl, 3-isothiazolin-5-yl,4-isothiazolin-5-yl, 2,3-dihydropyrazol-1-yl, 2,3-dihydropyrazol-2-yl,2,3-dihydropyrazol-3-yl, 2,3-dihydropyrazol-4-yl,2,3-dihydropyrazol-5-yl, 3,4-dihydropyrazol-1-yl,3,4-dihydropyrazol-3-yl, 3,4-dihydropyrazol-4-yl,3,4-dihydropyrazol-5-yl, 4,5-dihydropyrazol-1-yl,4,5-dihydropyrazol-3-yl, 4,5-dihydropyrazol-4-yl,4,5-dihydropyrazol-5-yl, 2,3-dihydrooxazol-2-yl, 2,3-dihydrooxazol-3-yl,2,3-dihydrooxazol-4-yl, 2,3-dihydrooxazol-5-yl, 3,4-dihydrooxazol-2-yl,3,4-dihydrooxazol-3-yl, 3,4-dihydrooxazol-4-yl, 3,4-dihydrooxazol-5-yl,3,4-dihydrooxazol-2-yl, 3,4-dihydrooxazol-3-yl, 3,4-dihydrooxazol-4-yl,2-piperidinyl, 3-piperidinyl, 4-piperidinyl, 1,3-dioxan-5-yl,2-tetrahydropyranyl, 4-tetrahydropyranyl, 2-tetrahydrothienyl,3-hexahydropyridazinyl, 4-hexa-hydropyridazinyl, 2-hexahydropyrimidinyl,4-hexahydropyrimidinyl, 5-hexahydropyrimidinyl, 2-piperazinyl,1,3,5-hexahydrotriazin-2-yl and 1,2,4-hexahydrotriazin-3-yl and also thecorresponding -ylidene radicals;

a five- or six-membered aromatic heterocyclyl (=heteroaromatic radical)which contains one, two, three or four heteroatoms from the groupconsisting of oxygen, nitrogen and sulfur, for example 5-memberedheteroaryl which is attached via carbon and contains one to threenitrogen atoms or one or two nitrogen atoms and one sulfur or oxygenatom as ring members, such as 2-furyl, 3-furyl, 2-thienyl, 3-thienyl,2-pyrrolyl, 3-pyrrolyl, 3-isoxazolyl, 4-isoxazolyl, 5-isoxazolyl,3-isothiazolyl, 4-isothiazolyl, 5-isothiazolyl, 3-pyrazolyl,4-pyrazolyl, 5-pyrazolyl, 2-oxazolyl, 4-oxazolyl, 5-oxazolyl,2-thiazolyl, 4-thiazolyl, 5-thiazolyl, 2-imidazolyl, 4-imidazolyl,1,2,4-oxadiazol-3-yl, 1,2,4-oxadiazol-5-yl, 1,2,4-thiadiazol-3-yl,1,2,4-thiadiazol-5-yl, 1,2,4-triazol-3-yl, 1,3,4-oxadiazol-2-yl,1,3,4-thiadiazol-2-yl and 1,3,4-triazol-2-yl; 5-membered heteroarylwhich is attached via nitrogen and contains one to three nitrogen atomsas ring members, such as pyrrol-1-yl, pyrazol-1-yl, imidazol-1-yl,1,2,3-triazol-1-yl and 1,2,4-triazol-1-yl; 6-membered heteroaryl, whichcontains one, two or three nitrogen atoms as ring members, such aspyridin-2-yl, pyridin-3-yl, pyridin-4-yl, 3-pyridazinyl, 4-pyridazinyl,2-pyrimidinyl, 4-pyrimidinyl, 5-pyrimidinyl, 2-pyrazinyl,1,3,5-triazin-2-yl and 1,2,4-triazin-3-yl.

The preferred embodiments of the invention mentioned herein below haveto be understood as being preferred either independently from each otheror in combination with one another.

According to a preferred embodiment of the invention preference is givento those compositions comprising an isoxazolo[5,4-b]pyridine of formulaI, wherein R¹ is hydrogen, halogen, C₁-C₆-alkyl or C₁-C₆-haloalkyl.Particularly preferred are those compositions comprising anisoxazolo[5,4-b]pyridine of formula I , wherein R¹ is hydrogen.

According to another preferred embodiment of the invention, preferenceis given to those compositions comprising an isoxazolo[5,4-b]pyridine offormula I, wherein R² is C₁-C₆-alkyl, C₁-C₆-haloalkyl,C₁-C₆-hydroxyalkyl, C₃-C₆-cycloalkyl, C₃-C₆-halocycloalkyl,C₂-C₆-alkenyl or C₂-C₆-alkynyl. Particularly preferred are thosecompositions comprising an isoxazolo[5,4-b]pyridine of formula I,wherein R² is C₃-C₆-cycloalkyl or C₃-C₆-halocycloalkyl; mostparticularly preferred are those compositions comprising anisoxazolo[5,4-b]pyridine of formula I, wherein R² is cyclopropyl or1-fluorocyclopropyl.

According to another preferred embodiment of the invention, preferenceis also given to those compositions comprising anisoxazolo[5,4-b]pyridine of formula I, wherein R³ is C₁-C₆-alkyl,C₁-C₆-haloalkyl, C₃-C₆-cycloalkyl-C₁-C₆-alkyl,C₃-C₆-halocycloalkyl-C₁-C₆-alkyl, C₃-C₆-cycloalkyl,C₃-C₆-halocycloalkyl, C₁-C₄-alkyl-C₃-C₆-cycloalkyl, C₁-C₆-alkoxy,C₁-C₆-haloalkoxy or phenyl; wherein the phenyl moieties of R³ can beunsubstituted or substituted with one or more radicals selected fromhalogen, hydroxy, nitro, cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl,C₁-C₄-alkoxy-C₁-C₄-alkyl, C₃-C₆-cycloalkyl, C₂-C₆-alkenyl,C₂-C₆-alkynyl, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy, C₁-C₄-alkoxycarbonyl,C₁-C₄-alkylthio, C₁-C₄-alkylsulfinyl, C₁-C₄-alkylsulfonyl, amino,C₁-C₄-alkylamino, N,N-di-(C₁-C₄)-alkylamino, heterocyclyl and phenyl.

Particularly preferred are those compositions comprising anisoxazolo[5,4-b]pyridine of formula I, wherein R³ is C₁-C₆-alkyl,C₁-C₆-haloalkyl, C₃-C₆-cycloalkyl-C₁-C₆-alkyl,C₃-C₆-halocycloalkyl-C₁-C₆-alkyl, C₃-C₆-cycloalkyl,C₃-C₆-halocycloalkyl, C₁-C₄-alkyl-C₃-C₆-cycloalkyl, C₁-C₆-alkoxy orC₁-C₆-haloalkoxy. In a very particularly preferred aspect R³ is methyl,cyclopropyl or 1,1-dimethylethoxy; even more particularly preferred R³is cyclopropyl.

Another preferred embodiment of the invention relates to compositionscomprising an isoxazolo[5,4-b]pyridine of formula I, wherein

R¹ is hydrogen;

R² is hydrogen, C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₁-C₆-hydroxyalkyl,C₃-C₆-cycloalkyl, C₃-C₆-halocycloalkyl, C₂-C₆-alkenyl or C₂-C₆-alkynyl;

R³ is hydrogen, halogen, hydroxy, C₁-C₆-alkyl, C₁-C₆-haloalkyl,C₁-C₆-hydroxyalkyl, C₁-C₆-alkoxy-C₁-C₆-alkyl,C₁-C₆-haloalkoxy-C₁-C₆-alkyl, C₃-C₆-cycloalkyl-C₁-C₆-alkyl,C₃-C₆-halocycloalkyl-C₁-C₆-alkyl, C₃-C₆-cycloalkyl,C₃-C₆-halocycloalkyl, C₁-C₄-alkyl-C₃-C₆-cycloalkyl, C₃-C₆-cycloalkenyl,C₃-C₆-halocycloalkenyl, phenyl-C₁-C₆-alkyl, heterocyclyl-C₁-C₆-alkyl,C₂-C₆-alkenyl, C₂-C₆-haloalkenyl, C₂-C₆-alkynyl, C₂-C₆-haloalkynyl,C₁-C₆-alkoxy, C₁-C₆-haloalkoxy, C₁-C₆-alkylthio, C₁-C₆-haloalkylthio,amino, C₁-C₆-alkylamino, N,N-di-(C₁-C₆)-alkylamino, heterocyclyl orphenyl; wherein the heterocyclyl and phenyl moieties of R³ can beunsubstituted or substituted with one or more radicals selected fromhalogen, hydroxy, nitro, cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl,C₁-C₄-alkoxy-C₁-C₄-alkyl, C₃-C₆-cycloalkyl, C₂-C₆-alkenyl,C₂-C₆-alkynyl, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy, C₁-C₄-alkoxycarbonyl,C₁-C₄-alkylthio, C₁-C₄-alkylsulfinyl, C₁-C₄-alkylsulfonyl, amino,C₁-C₄-alkylamino, N,N-di-(C₁-C₄)-alkylamino, heterocyclyl and phenyl;

or its agriculturally acceptable salt, carboxylic ester, thioester oramide.

A further preferred embodiment of the invention relates to compositionscomprising an isoxazolo[5,4-b]pyridine of formula I, wherein

R¹ is hydrogen;

R² is hydrogen, C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₁-C₆-hydroxyalkyl,C₃-C₆-cycloalkyl, C₃-C₆-halocycloalkyl, C₂-C₆-alkenyl or C₂-C₆-alkynyl;

R³ is C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₃-C₆-cycloalkyl-C₁-C₆-alkyl,C₃-C₆-halocycloalkyl-C₁-C₆-alkyl, C₃-C₆-cycloalkyl,C₃-C₆-halocycloalkyl, C₁-C₄-alkyl-C₃-C₆-cycloalkyl, C₁-C₆-alkoxy,C₁-C₆-haloalkoxy or phenyl; wherein the phenyl moieties of R³ can beunsubstituted or substituted with one or more radicals selected fromhalogen, hydroxy, nitro, cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl,C₁-C₄-alkoxy-C₁-C₄-alkyl, C₃-C₆-cycloalkyl, C₂-C₆-alkenyl,C₂-C₆-alkynyl, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy, C₁-C₄-alkoxycarbonyl,C₁-C₄-alkylthio, C₁-C₄-alkynyl, alkylsulfinyl, C₁-C₄-alkylsulfonyl,amino, C₁-C₄-alkylamino, N,N-di-(C₁-C₄)-alkylamino, heterocyclyl andphenyl;

or its agriculturally acceptable salt, carboxylic ester, thioester oramide.

One preferred aspect of the invention relates to compositions comprisingan isoxazolo[5,4-b]pyridine of formula I, wherein

R¹ is hydrogen;

R² is C₃-C₆-cycloalkyl or C₃-C₆-halocycloalkyl; most preferablycyclopropyl or 1-fluorocyclopropyl;

R³ is hydrogen, halogen, hydroxy, C₁-C₆-alkyl, C₁-C₆-haloalkyl,C₁-C₆-hydroxyalkyl, C₁-C₆-alkoxy-C₁-C₆-alkyl,C₁-C₆-haloalkoxy-C₁-C₆-alkyl, C₃-C₆-cycloalkyl-C₁-C₆-alkyl,C₃-C₆-halocycloalkyl-C₁-C₆-alkyl, C₃-C₆-cycloalkyl,C₃-C₆-halocycloalkyl, C₁-C₄-alkyl-C₃-C₆-cycloalkyl, C₃-C₆-cycloalkenyl,C₃-C₆-halocycloalkenyl, phenyl-C₁-C₆-alkyl, heterocyclyl-C₁-C₆-alkyl,C₂-C₆-alkenyl, C₂-C₆-haloalkenyl, C₂-C₆-alkynyl, C₂-C₆-haloalkynyl,C₁-C₆-alkoxy, C₁-C₆-haloalkoxy, C₁-C₆-alkylthio, C₁-C₆-haloalkylthio,amino, C₁-C₆-alkylamino, N,N-di-(C₁-C₆)-alkylamino, heterocyclyl orphenyl; wherein the heterocyclyl and phenyl moieties of R³ can beunsubstituted or substituted with one or more radicals selected fromhalogen, hydroxy, nitro, cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl,C₁-C₄-alkoxy-C₁-C₄-alkyl, C₃-C₆-cycloalkyl, C₂-C₆-alkenyl,C₂-C₆-alkynyl, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy, C₁-C₄-alkoxycarbonyl,C₁-C₄-alkylthio, C₁-C₄-alkylsulfinyl, C₁-C₄-alkylsulfonyl, amino,C₁-C₄-alkylamino, N,N-di-(C₁-C₄)-alkylamino, heterocyclyl and phenyl;

or its agriculturally acceptable salt, carboxylic ester, thioester oramide.

Another preferred aspect of the invention relates to compositionscomprising an isoxazolo[5,4-b]pyridine of formula I, wherein

R¹ is hydrogen;

R² is C₃-C₆-cycloalkyl or C₃-C₆-halocycloalkyl; most preferablycyclopropyl or 1-fluorocyclopropyl;

R³ is C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₃-C₆-cycloalkyl-C₁-C₆-alkyl,C₃-C₆-halocycloalkyl-C₁-C₆-alkyl, C₃-C₆-cycloalkyl, C₃-C₆-halocycloalkylor C₁-C₄-alkyl-C₃-C₆-cycloalkyl, C₁-C₆-alkoxy, C₁-C₆-haloalkoxy orphenyl; wherein the phenyl moieties of R³ can be unsubstituted orsubstituted with one or more radicals selected from halogen, hydroxy,nitro, cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy-C₁-C₄-alkyl,C₃-C₆-cycloalkyl, C₂-C₆-alkenyl, C₂-C₆-alkynyl, C₁-C₄-alkoxy,C₁-C₄-haloalkoxy, C₁-C₄-alkoxycarbonyl, C₁-C₄-alkylthio,C₁-C₄-alkylsulfinyl, C₁-C₄-alkylsulfonyl, amino, C₁-C₄-alkylamino,N,N-di-(C₁-C₄)-alkylamino, heterocyclyl, and phenyl;

or its agriculturally acceptable salt, carboxylic ester, thioester oramide.

Still another more preferred embodiment of the invention relates tocompositions comprising an isoxazolo[5,4-b]pyridine of formula I,wherein

R¹ is hydrogen;

R² is C₃-C₆-cycloalkyl or C₃-C₆-halocycloalkyl; most preferablycyclopropyl or 1-fluorocyclopropyl;

R³ is C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₃-C₆-cycloalkyl-C₁-C₆-alkyl,C₃-C₆-halocycloalkyl-C₁-C₆-alkyl, C₃-C₆-cycloalkyl,C₃-C₆-halocycloalkyl, C₁-C₄-alkyl-C₃-C₆-cycloalkyl, C₁-C₆-alkoxy orC₁-C₆-haloalkoxy;

or its agriculturally acceptable salt, carboxylic ester, thioester oramide.

Still another more preferred embodiment of the invention relates tocompositions comprising an isoxazolo[5,4-b]pyridine of formula I,wherein

R¹ is hydrogen;

R² is C₃-C₆-cycloalkyl or C₃-C₆-halocycloalkyl; most preferablycyclopropyl or 1-fluorocyclopropyl;

R³ is C₁-C₆-alkyl, C₃-C₆-cycloalkyl or C₁-C₆-alkoxy;

or its agriculturally acceptable salt, carboxylic ester, thioester oramide.

A further more preferred embodiment of the invention relates tocompositions comprising an isoxazolo[5,4-b]pyridine of formula I,wherein

R¹ is hydrogen;

R² is cyclopropyl;

R³ is C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₃-C₆-cycloalkyl-C₁-C₆-alkyl,C₃-C₆-halocycloalkyl-C₁-C₆-alkyl, C₃-C₆-cycloalkyl,C₃-C₆-halocycloalkyl, C₁-C₄-alkyl-C₃-C₆-cycloalkyl, C₁-C₆-alkoxy,C₁-C₆-haloalkoxy or phenyl; wherein the phenyl moieties of R³ can beunsubstituted or substituted with one or more radicals selected fromhalogen, hydroxy, nitro, cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl,C₁-C₄-alkoxy-C₁-C₄-alkyl, C₃-C₆-cycloalkyl, C₂-C₆-alkenyl,C₂-C₆-alkynyl, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy, C₁-C₄-alkoxycarbonyl,C₁-C₄-alkylthio, C₁-C₄-alkylsulfinyl, C₁-C₄-alkylsulfonyl, amino,C₁-C₄-alkylamino, N,N-di-(C₁-C₄)-alkylamino, heterocyclyl and phenyl;

or its agriculturally acceptable salt, carboxylic ester, thioester oramide.

Still another more preferred embodiment of the invention relates tocompositions comprising an isoxazolo[5,4-b]pyridine of formula I,wherein

R¹ is hydrogen;

R² is C₃-C₆-cycloalkyl;

R³ is C₁-C₆-alkyl, C₃-C₆-cycloalkyl or C₁-C₆-alkoxy;

or its agriculturally acceptable salt, carboxylic ester, thioester oramide.

Still another more preferred embodiment of the invention relates tocompositions comprising an isoxazolo[5,4-b]pyridine of formula I,wherein

R¹ is hydrogen;

R² is cyclopropyl;

R³ is cyclopropyl, methyl or 1,1-dimethylethoxy;

or its agriculturally acceptable salt, carboxylic ester, thioester oramide.

According to a particular preferred embodiment of the invention thecomposition comprises as component A an isoxazolo[5,4-b]pyridine offormula (I.1) or its agriculturally acceptable salt, carboxylic ester,thioester or amide.

According to a further particular preferred embodiment of the inventionthe composition comprises as component A an isoxazolo[5,4-b]pyridine offormula (I.2) or its agriculturally acceptable salt, carboxylic ester,thioester or amide.

According to a further particular preferred embodiment of the inventionthe composition comprises as component A an isoxazolo[5,4-b]pyridine offormula (I.3) and its agriculturally acceptable salt, carboxylic ester,thioester or amide.

In one embodiment of the present invention the compositions according tothe present invention comprise as component A at least oneisoxazolo[5,4-b]pyridine of formula (I) and at least one furtherherbicide B as component B.

According to a first embodiment of the invention the compositionscomprise at least one inhibitor of the lipid biosynthesis (herbicideb1). These are compounds that inhibit lipid biosynthesis. Inhibition ofthe lipid biosynthesis can be affected either through inhibition ofacetylCoA carboxylase (hereinafter termed ACC herbicides) or through adifferent mode of action (hereinafter termed non-ACC herbicides). TheACC herbicides belong to the group A of the HRAC classification systemwhereas the non-ACC herbicides belong to the group N of the HRACclassification.

According to a second embodiment of the invention the compositionscomprise at least one ALS inhibitor (herbicide b2). The herbicidalactivity of these compounds is based on the inhibition of acetolactatesynthase and thus on the inhibition of the branched chain amino acidbiosynthesis. These inhibitors belong to the group B of the HRACclassification system.

According to a third embodiment of the invention the compositionscomprise at least one inhibitor of photosynthesis (herbicide b3). Theherbicidal activity of these compounds is based either on the inhibitionof the photosystem II in plants (so-called PSII inhibitors, groups C1,C2 and C3 of HRAC classification) or on diverting the electron transferin photosystem I in plants (so-called PSI inhibitors, group D of HRACclassification) and thus on an inhibition of photosynthesis. Amongstthese, PSII inhibitors are preferred.

According to a fourth embodiment of the invention the compositionscomprise at least one inhibitor of protoporphyrinogen-IX-oxidase(herbicide b4). The herbicidal activity of these compounds is based onthe inhibition of the protoporphyrinogen-IX-oxidase. These inhibitorsbelong to the group E of the HRAC classification system.

According to a fifth embodiment of the invention the compositionscomprise at least one bleacher-herbicide (herbicide b5). The herbicidalactivity of these compounds is based on the inhibition of the carotenoidbiosynthesis. These include compounds which inhibit carotenoidbiosynthesis by inhibition of phytoene desaturase (so-called PDSinhibitors, group F1 of HRAC classification), compounds that inhibit the4-hydroxyphenylpyruvate-dioxygenase (HPPD inhibitors, group F2 of HRACclassification), compounds that inhibit DOXsynthase (group F4 of HRACclass) and compounds which inhibit carotenoid biosynthesis by an unknownmode of action (bleacher—unknown target, group F3 of HRACclassification).

According to a sixth embodiment of the invention the compositionscomprise at least one EPSP synthase inhibitor (herbicide b6). Theherbicidal activity of these compounds is based on the inhibition ofenolpyruvyl shikimate 3-phosphate synthase, and thus on the inhibitionof the amino acid biosynthesis in plants. These inhibitors belong to thegroup G of the HRAC classification system.

According to a seventh embodiment of the invention the compositionscomprise at least one glutamine synthetase inhibitor (herbicide b7). Theherbicidal activity of these compounds is based on the inhibition ofglutamine synthetase, and thus on the inhibition of the aminoacidbiosynthesis in plants. These inhibitors belong to the group H of theHRAC classification system.

According to an eighth embodiment of the invention the compositionscomprise at least one DHP synthase inhibitor (herbicide b8). Theherbicidal activity of these compounds is based on the inhibition of7,8-dihydropteroate synthase. These inhibitors belong to the group I ofthe HRAC classification system.

According to a ninth embodiment of the invention the compositionscomprise at least one mitosis inhibitor (herbicide b9). The herbicidalactivity of these compounds is based on the disturbance or inhibition ofmicrotubule formation or organization, and thus on the inhibition ofmitosis. These inhibitors belong to the groups K1 and K2 of the HRACclassification system. Among these, compounds of the group K1, inparticular dinitroanilines, are preferred.

According to a tenth embodiment of the invention the compositionscomprise at least one VLCFA inhibitor (herbicide b10). The herbicidalactivity of these compounds is based on the inhibition of the synthesisof very long chain fatty acids and thus on the disturbance or inhibitionof cell division in plants. These inhibitors belong to the group K3 ofthe HRAC classification system.

According to an eleventh embodiment of the invention the compositionscomprise at least one cellulose biosynthesis inhibitor (herbicide b11).The herbicidal activity of these compounds is based on the inhibition ofthe biosynthesis of cellulose and thus on the inhibition of thesynthesis of cell walls in plants. These inhibitors belong to the groupL of the HRAC classification system.

According to a twelfth embodiment of the invention the compositionscomprise at least one decoupler herbicide (herbicide b12). Theherbicidal activity of these compounds is based on the disruption of thecell membrane. These inhibitors belong to the group M of the HRACclassification system.

According to a thirtheenth embodiment of the invention the compositionscomprise at least one auxinic herbicide (herbicide b13). These includecompounds that mimic auxins, i.e. plant hormones, and affect the growthof the plants. These compounds belong to the group O of the HRACclassification system.

According to a fourteenth embodiment of the invention the compositionscomprise at least one auxin transport inhibitor (herbicide b14). Theherbicidal activity of these compounds is based on the inhibition of theauxin transport in plants. These compounds belong to the group P of theHRAC classification system.

As to the given mechanisms of action and classification of the activesubstances, see e.g. “HRAC, Classification of Herbicides According toMode of Action”, http://www.plantprotection.org/hrac/MOA.html).

Preference is given to those compositions according to the presentinvention comprising as component B at least one herbicide B selectedfrom herbicides of the classes b1, b2, b3, b4, b5, b6, b10 and b13.

Specific preference is given to those compositions according to thepresent invention which comprise as component B at least one herbicide Bselected from the herbicides of the classes b2, b3, b4, b5, b6 and b13.

Particular preference is given to those compositions according to thepresent invention which comprise as component B at least one herbicide Bselected from the herbicides of the classes b2, b3, b5 and b13.

Examples of herbicides B which can be used in combination with anisoxazolo[5,4-b]pyridine of formula (I) according to the presentinvention are:

b1) from the group of the lipid biosynthesis inhibitors:

ACC-herbicides such as alloxydim, alloxydim-sodium, butroxydim,clethodim, clodinafop, clodinafop-propargyl, cycloxydim, cyhalofop,cyhalofop-butyl, diclofop, diclofop-methyl, fenoxaprop,fenoxaprop-ethyl, fenoxaprop-P, fenoxaprop-P-ethyl, fluazifop,fluazifop-butyl, fluazifop-P, fluazifop-P-butyl, haloxyfop,haloxyfop-methyl, haloxyfop-P, haloxyfop-P-methyl, metamifop, pinoxaden,profoxydim, propaquizafop, quizalofop, quizalofop-ethyl,quizalofop-tefuryl, quizalofop-P, quizalofop-P-ethyl,quizalofop-P-tefuryl, sethoxydim, tepraloxydim, tralkoxydim,4-(4′-Chloro-4-cyclopropyl-2′-fluoro[1,1′-biphenyl]-3-yl)-5-hydroxy-2,2,6,6-tetramethyl-2H-pyran-3(6H)-one(CAS 1312337-72-6);4-(2′,4′-Dichloro-4-cyclopropyl[1,1′-biphenyl]-3-yl)-5-hydroxy-2,2,6,6-tetramethyl-2H-pyran-3(6H)-one(CAS 1312337-45-3);4-(4′-Chloro-4-ethyl-2′-fluoro[1,1′-biphenyl]-3-yl)-5-hydroxy-2,2,6,6-tetramethyl-2H-pyran-3(6H)-one(CAS 1033757-93-5);4-(2′,4′-Dichloro-4-ethyl[1,1′-biphenyl]-3-yl)-2,2,6,6-tetramethyl-2H-pyran-3,5(4H,6H)-dione(CAS 1312340-84-3);5-(Acetyloxy)-4-(4′-chloro-4-cyclopropyl-2′-fluoro[1,1′-biphenyl]-3-yl)-3,6-dihydro-2,2,6,6-tetramethyl-2H-pyran-3-one(CAS 1312337-48-6);5-(Acetyloxy)-4-(2″,4′-dichloro-4-cyclopropyl-[1,1′-biphenyl]-3-yl)-3,6-dihydro-2,2,6,6-tetramethyl-2H-pyran-3-one;5-(Acetyloxy)-4-(4′-chloro-4-ethyl-2′-fluoro[1,1′-biphenyl]-3-yl)-3,6-dihydro-2,2,6,6-tetramethyl-2H-pyran-3-one(CAS 1312340-82-1);5-(Acetyloxy)-4-(2′,4′-dichloro-4-ethyl[1,1′-biphenyl]-3-yl)-3,6-dihydro-2,2,6,6-tetramethyl-2H-pyran-3-one(CAS 1033760-55-2);4-(4′-Chloro-4-cyclopropyl-2′-fluoro[1,1′-biphenyl]-3-yl)-5,6-dihydro-2,2,6,6-tetramethyl-5-oxo-2H-pyran-3-ylcarbonic acid methyl ester (CAS 1312337-51-1); 4-(2″,4′-Dichloro-4-cyclopropyl-[1,1′-biphenyl]-3-yl)-5,6-dihydro-2,2,6,6-tetramethyl-5-oxo-2H-pyran-3-ylcarbonic acid methyl ester;4-(4′-Chloro-4-ethyl-2′-fluoro[1,1′-biphenyl]-3-yl)-5,6-dihydro-2,2,6,6-tetramethyl-5-oxo-2H-pyran-3-ylcarbonic acid methyl ester (CAS 1312340-83-2);4-(2′,4′-Dichloro-4-ethyl[1,1′-biphenyl]-3-yl)-5,6-dihydro-2,2,6,6-tetramethyl-5-oxo-2H-pyran-3-ylcarbonic acid methyl ester (CAS 1033760-58-5); and non ACC herbicidessuch as benfuresate, butylate, cycloate, dalapon, dimepiperate, EPTC,esprocarb, ethofumesate, flupropanate, molinate, orbencarb, pebulate,prosulfocarb, TCA, thiobencarb, tiocarbazil, triallate and vernolate;

b2) from the group of the ALS inhibitors:

sulfonylureas such as amidosulfuron, azimsulfuron, bensulfuron,bensulfuron-methyl, chlorimuron, chlorimuron-ethyl, chlorsulfuron,cinosulfuron, cyclosulfamuron, ethametsulfuron, ethametsulfuron-methyl,ethoxysulfuron, flazasulfuron, flucetosulfuron, flupyrsulfuron,flupyrsulfuron-methyl-sodium, foramsulfuron, halosulfuron,halosulfuron-methyl, imazosulfuron, iodosulfuron,iodosulfuron-methyl-sodium, iofensulfuron, iofensulfuron-sodium,mesosulfuron, metazosulfuron, metsulfuron, metsulfuron-methyl,nicosulfuron, orthosulfamuron, oxasulfuron, primisulfuron,primisulfuron-methyl, propyrisulfuron, prosulfuron, pyrazosulfuron,pyrazosulfuron-ethyl, rimsulfuron, sulfometuron, sulfometuron-methyl,sulfosulfuron, thifensulfuron, thifensulfuron-methyl, triasulfuron,tribenuron, tribenuron-methyl, trifloxysulfuron, triflusulfuron,triflusulfuron-methyl and tritosulfuron,

imidazolinones such as imazamethabenz, imazamethabenz-methyl, imazamox,imazapic, imazapyr, imazaquin and imazethapyr, triazolopyrimidineherbicides and sulfonanilides such as cloransulam, cloransulam-methyl,diclosulam, flumetsulam, florasulam, metosulam, penoxsulam, pyrimisulfanand pyroxsulam,

pyrimidinylbenzoates such as bispyribac, bispyribac-sodium,pyribenzoxim, pyriftalid, pyriminobac, pyriminobac-methyl, pyrithiobac,pyrithiobac-sodium,4-[[[2-[(4,6-dimethoxy-2-pyrimidinyl)oxy]phenyl]methyl]amino]-benzoicacid-1-methylethyl ester (CAS 420138-41-6),4-[[[2-[(4,6-dimethoxy-2-pyrimidinyl)oxy]phenyl]methyl]amino]-benzoicacid propyl ester (CAS 420138-40-5),N-(4-bromophenyl)-2-[(4,6-dimethoxy-2-pyrimidinyl)oxy]benzenemethanamine(CAS 420138-01-8),

sulfonylaminocarbonyl-triazolinone herbicides such as flucarbazone,flucarbazone-sodium, propoxycarbazone, propoxycarbazone-sodium,thiencarbazone and thiencarbazone-methyl; and triafamone;

among these, a preferred embodiment of the invention relates to thosecompositions comprising at least one imidazolinone herbicide;

b3) from the group of the photosynthesis inhibitors:

amicarbazone, inhibitors of the photosystem II, e.g. triazineherbicides, including of chlorotriazine, triazinones, triazindiones,methylthiotriazines and pyridazinones such as ametryn, atrazine,chloridazone, cyanazine, desmetryn, dimethametryn, hexazinone,metribuzin, prometon, prometryn, propazine, simazine, simetryn,terbumeton, terbuthylazin, terbutryn and trietazin, aryl urea such aschlorobromuron, chlorotoluron, chloroxuron, dimefuron, diuron,fluometuron, isoproturon, isouron, linuron, metamitron,methabenzthiazuron, metobenzuron, metoxuron, monolinuron, neburon,siduron, tebuthiuron and thiadiazuron, phenyl carbamates such asdesmedipham, karbutilat, phenmedipham, phenmedipham-ethyl, nitrileherbicides such as bromofenoxim, bromoxynil and its salts and esters,ioxynil and its salts and esters, uraciles such as bromacil, lenacil andterbacil, and bentazon and bentazon-sodium, pyridate, pyridafol,pentanochlor and propanil and inhibitors of the photosystem I such asdiquat, diquat-dibromide, paraquat, paraquat-dichloride andparaquat-dimetilsulfate. Among these, a preferred embodiment of theinvention relates to those compositions comprising at least one arylurea herbicide. Among these, likewise a preferred embodiment of theinvention relates to those compositions comprising at least one triazineherbicide. Among these, likewise a preferred embodiment of the inventionrelates to those compositions comprising at least one nitrile herbicide;

b4) from the group of the protoporphyrinogen-IX oxidase inhibitors:

acifluorfen, acifluorfen-sodium, azafenidin, bencarbazone,benzfendizone, bifenox, butafenacil, carfentrazone, carfentrazone-ethyl,chlomethoxyfen, cinidon-ethyl, fluazolate, flufenpyr, flufenpyr-ethyl,flumiclorac, flumiclorac-pentyl, flumioxazin, fluoroglycofen,fluoroglycofen-ethyl, fluthiacet, fluthiacet-methyl, fomesafen,halosafen, lactofen, oxadiargyl, oxadiazon, oxyfluorfen, pentoxazone,profluazol, pyraclonil, pyraflufen, pyraflufen-ethyl, saflufenacil,sulfentrazone, thidiazimin, tiafenacil, trifludimoxazin, ethyl[3-[2-chloro-4-fluoro-5-(1-methyl-6-trifluoromethyl-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-3-yl)phenoxy]-2-pyridyloxy]acetate(CAS 353292-31-6; S-3100,N-ethyl-3-(2,6-dichloro-4-trifluoro-methylphenoxy)-5-methyl-1H-pyrazole-1-carboxamide(CAS 452098-92-9),N-tetrahydrofurfuryl-3-(2,6-dichloro-4-trifluoromethylphenoxy)-5-methyl-1H-pyrazole-1-carboxamide(CAS 915396-43-9),N-ethyl-3-(2-chloro-6-fluoro-4-trifluoromethylphenoxy)-5-methyl-1H-pyrazole-1-carboxamide(CAS 452099-05-7),N-tetrahydrofurfuryl-3-(2-chloro-6-fluoro-4-trifluoromethylphenoxy)-5-methyl-1H-pyrazole-1-carboxamide(CAS 452100-03-7),3-[7-fluoro-3-oxo-4-(prop-2-ynyl)-3,4-dihydro-2H-benzo[1,4]oxazin-6-yl]-1,5-dimethyl-6-thioxo-[1,3,5]triazinan-2,4-dione,2-(2,2,7-trifluoro-3-oxo-4-prop-2-ynyl-3,4-dihydro-2H-benzo[1,4]oxazin-6-yl)-4,5,6,7-tetrahydro-isoindole-1,3-dione(CAS 1300118-96-0,1-Methyl-6-trifluoromethyl-3-(2,2,7-trifluoro-3-oxo-4-prop-2-ynyl-3,4-dihydro-2H-benzo[1,4]oxazin-6-yl)-1H-pyrimidine-2,4-dione(CAS 1304113-05-0), methyl(E)-4-[2-chloro-5-[4-chloro-5-(difluoromethoxy)-1H-methyl-pyrazol-3-yl]-4-fluoro-phenoxy]-3-methoxy-but-2-enoate[CAS 948893-00-3], and3-[7-Chloro-5-fluoro-2-(trifluoromethyl)-1H-benzimidazol-4-yl]-1-methyl-6-(trifluoromethyl)-1H-pyrimidine-2,4-dione(CAS 212754-02-4);

b5) from the group of the bleacher herbicides:

PDS inhibitors: beflubutamid, diflufenican, fluridone, flurochloridone,flurtamone, norflurazon, picolinafen, and4-(3-trifluoromethylphenoxy)-2-(4-trifluoromethylphenyl)-pyrimidine (CAS180608-33-7), HPPD inhibitors: benzobicyclon, benzofenap, bicyclopyrone,clomazone, fenquinotrione, isoxaflutole, mesotrione, pyrasulfotole,pyrazolynate, pyrazoxyfen, sulcotrione, tefuryltrione, tembotrione,tolpyralate, topramezone, bleacher, unknown target: aclonifen, amitroleand flumeturon;

b6) from the group of the EPSP synthase inhibitors:

glyphosate, glyphosate-isopropylammonium, glyposate-potassium andglyphosate-trimesium (sulfosate);

b7) from the group of the glutamine synthase inhibitors:

bilanaphos (bialaphos), bilanaphos-sodium, glufosinate, glufosinate-Pand glufosinate-ammonium;

b8) from the group of the DHP synthase inhibitors:

asulam;

b9) from the group of the mitosis inhibitors:

compounds of group K1: dinitroanilines such as benfluralin, butralin,dinitramine, ethalfluralin, fluchloralin, oryzalin, pendimethalin,prodiamine and trifluralin, phosphoramidates such as amiprophos,amiprophos-methyl, and butamiphos, benzoic acid herbicides such aschlorthal, chlorthal-dimethyl, pyridines such as dithiopyr andthiazopyr, benzamides such as propyzamide and tebutam; compounds ofgroup K2: carbetamide, chlorpropham, flamprop, flamprop-isopropyl,flamprop-methyl, flamprop-M-isopropyl and propham, among these,compounds of group K1, in particular dinitroanilines are preferred;

b10) from the group of the VLCFA inhibitors:

chloroacetamides such as acetochlor, alachlor, butachlor, dimethachlor,dimethenamid, dimethenamid-P, metazachlor, metolachlor, metolachlor-S,pethoxamid, pretilachlor, propachlor, propisochlor and thenylchlor,oxyacetanilides such as flufenacet and mefenacet, acetanilides such asdiphenamid, naproanilide, napropamide and napropamide-M, tetrazolinonessuch fentrazamide, and other herbicides such as anilofos, cafenstrole,fenoxasulfone, ipfencarbazone, piperophos, pyroxasulfone and isoxazolinecompounds of the formulae II.1, II.2, II.3, II.4, II.5, II.6, II.7, II.8and II.9

the isoxazoline compounds of the formula (I)I are known in the art, e.g.from WO 2006/024820, WO 2006/037945, WO 2007/071900 and WO 2007/096576;

among the VLCFA inhibitors, preference is given to chloroacetamides andoxyacetamides;

b11) from the group of the cellulose biosynthesis inhibitors:

chlorthiamid, dichlobenil, flupoxam, indaziflam, isoxaben, triaziflamand 1-cyclohexyl-5-pentafluorphenyloxy-1⁴-[1,2,4,6]thiatriazin-3-ylamine(CAS 175899-01-1);

b12) from the group of the decoupler herbicides:

dinoseb, dinoterb and DNOC and its salts;

b13) from the group of the auxinic herbicides:

2,4-D and its salts and esters such as clacyfos, 2,4-DB and its saltsand esters, aminocyclopyrachlor and its salts and esters, aminopyralidand its salts such as aminopyralid-dimethylammonium,aminopyralid-tris(2-hydroxypropyl)ammonium and its esters, benazolin,benazolin-ethyl, chloramben and its salts and esters, clomeprop,clopyralid and its salts and esters, dicamba and its salts and esters,dichlorprop and its salts and esters, dichlorprop-P and its salts andesters, fluroxypyr, fluroxypyr-butometyl, fluroxypyr-meptyl, halauxifenand its salts and esters (CAS 943832-60-8), e.g. halauxifen-methyl, MCPAand its salts and esters, MCPA-thioethyl, MCPB and its salts and esters,mecoprop and its salts and esters, mecoprop-P and its salts and esters,picloram and its salts and esters, quinclorac, quinmerac, TBA (2,3,6)and its salts and esters and triclopyr and its salts and esters,4-amino-3-chloro-6-(4-chloro-2-fluoro-3-methoxyphenyl)-5-fluoropyridine-2-carboxylicacid and its salts and esters, e.g. benzyl4-amino-3-chloro-6-(4-chloro-2-fluoro-3-methoxyphenyl)-5-fluoropyridine-2-carboxylate(CAS 1390661-72-9);

b14) from the group of the auxin transport inhibitors: diflufenzopyr,diflufenzopyr-sodium, naptalam and naptalam-sodium;

b15) from the group of the other herbicides: bromobutide, chlorflurenol,chlorflurenol-methyl, (1RS,2SR,4SR)-1,4-epoxy-p-menth-2-yl2-methylbenzylether, cumyluron, cyclopyrimorate (CAS 499223-49-3) and its salts andesters, dalapon, dazomet, difenzoquat, difenzoquat-metilsulfate,dimethipin, DSMA, dymron, endothal and its salts, etobenzanid, flurenol,flurenol-butyl, flurprimidol, fosamine, fosamine-ammonium, indanofan,maleic hydrazide, mefluidide, metam, methiozolin (CAS 403640-27-7),methyl azide, methyl bromide, methyl-dymron, methyl iodide, MSMA, oleicacid, oxaziclomefone, pelargonic acid, pyributicarb, quinoclamine andtridiphane.

Preferred herbicides B that can be used in combination with anisoxazolo[5,4-b]pyridine of the formula (I) according to the presentinvention are:

b1) from the group of the lipid biosynthesis inhibitors:

clethodim, clodinafop-propargyl, cycloxydim, cyhalofop-butyl,diclofop-methyl, fenoxaprop-P-ethyl, fluazifop-P-butyl,haloxyfop-P-methyl, metamifop, pinoxaden, profoxydim, propaquizafop,quizalofop-P-ethyl, quizalofop-P-tefuryl, sethoxydim, tepraloxydim,tralkoxydim,4-(4′-Chloro-4-cyclopropyl-2′-fluoro[1,1′-biphenyl]-3-yl)-5-hydroxy-2,2,6,6-tetramethyl-2H-pyran-3(6H)-one(CAS 1312337-72-6);4-(2′,4′-Dichloro-4-cyclopropyl[1,1′-biphenyl]-3-yl)-5-hydroxy-2,2,6,6-tetramethyl-2H-pyran-3(6H)-one(CAS 1312337-45-3);4-(4′-Chloro-4-ethyl-2′-fluoro[1,1′-biphenyl]-3-yl)-5-hydroxy-2,2,6,6-tetramethyl-2H-pyran-3(6H)-one(CAS 1033757-93-5);4-(2′,4′-Dichloro-4-ethyl[1,1′-biphenyl]-3-yl)-2,2,6,6-tetramethyl-2H-pyran-3,5(4H,6H)-dione(CAS 1312340-84-3);5-(Acetyloxy)-4-(4′-chloro-4-cyclopropyl-2′-fluoro[1,1′-biphenyl]-3-yl)-3,6-dihydro-2,2,6,6-tetramethyl-2H-pyran-3-one(CAS 1312337-48-6);5-(Acetyloxy)-4-(2″,4′-dichloro-4-cyclopropyl-[1,1′-biphenyl]-3-yl)-3,6-dihydro-2,2,6,6-tetramethyl-2H-pyran-3-one;5-(Acetyloxy)-4-(4′-chloro-4-ethyl-2′-fluoro[1,1′-biphenyl]-3-yl)-3,6-dihydro-2,2,6,6-tetramethyl-2H-pyran-3-one(CAS 1312340-82-1);5-(Acetyloxy)-4-(2′,4′-dichloro-4-ethyl[1,1′-biphenyl]-3-yl)-3,6-dihydro-2,2,6,6-tetramethyl-2H-pyran-3-one(CAS 1033760-55-2);4-(4′-Chloro-4-cyclopropyl-2′-fluoro[1,1′-biphenyl]-3-yl)-5,6-dihydro-2,2,6,6-tetramethyl-5-oxo-2H-pyran-3-ylcarbonic acid methyl ester (CAS 1312337-51-1); 4-(2″,4′-Dichloro-4-cyclopropyl-[1,1′-biphenyl]-3-yl)-5,6-dihydro-2,2,6,6-tetramethyl-5-oxo-2H-pyran-3-ylcarbonic acid methyl ester;4-(4′-Chloro-4-ethyl-2′-fluoro[1,1′-biphenyl]-3-yl)-5,6-dihydro-2,2,6,6-tetramethyl-5-oxo-2H-pyran-3-ylcarbonic acid methyl ester (CAS 1312340-83-2);4-(2′,4′-Dichloro-4-ethyl[1,1′-biphenyl]-3-yl)-5,6-dihydro-2,2,6,6-tetramethyl-5-oxo-2H-pyran-3-ylcarbonic acid methyl ester (CAS 1033760-58-5); benfuresate,dimepiperate, EPTC, esprocarb, ethofumesate, molinate, orbencarb,prosulfocarb, thiobencarb and triallate;

More preferred herbicides B that can be used in combination with anisoxazolo[5,4-b]pyridine of the formula (I) according to the presentinvention are selected from the group b1) clodinafop-propargyl,cyhalofop-butyl, fluazifop-P-butyl, fenoxaprop-P-ethyl,haloxyfop-P-methyl, metamifop, propaquizafop, quizalofop-P-methyl,quizalofop-P-tefuryl, clethodim, cycloxydim, sethoxydim, profoxydim,tepraloxydim, tralkoxydim, pinoxaden, molinate and tri-allate.

b2) from the group of the ALS inhibitors:

amidosulfuron, azimsulfuron, bensulfuron-methyl, bispyribac-sodium,chlorimuron-ethyl, chlorsulfuron, cloransulam-methyl, cyclosulfamuron,diclosulam, ethametsulfuron-methyl, ethoxysulfuron, flazasulfuron,florasulam, flucarbazone-sodium, flucetosulfuron, flumetsulam,flupyrsulfuron-methyl-sodium, foramsulfuron, halosulfuron-methyl,imazamethabenz-methyl, imazamox, imazapic, imazapyr, imazaquin,imazethapyr, imazosulfuron, iodosulfuron, iodosulfuron-methyl-sodium,iofensulfuron, iofensulfuron-sodium, mesosulfuron, metazosulfuron,metosulam, metsulfuron-methyl, nicosulfuron, orthosulfamuron,oxasulfuron, penoxsulam, primisulfuron-methyl, propoxycarbazon-sodium,propyrisulfuron, prosulfuron, pyrazosulfuron-ethyl, pyribenzoxim,pyrimisulfan, pyriftalid, pyriminobac-methyl, pyrithiobac-sodium,pyroxsulam, rimsulfuron, sulfometuron-methyl, sulfosulfuron,thiencarbazone-methyl, thifensulfuron-methyl, triasulfuron,tribenuron-methyl, trifloxysulfuron, triflusulfuron-methyl,tritosulfuron and triafamone.

More preferred herbicides B from the group b2) that can be used incombination with an isoxazolo[5,4-b]pyridine of the formula (I)according to the present invention are selected from imazamox, imazapyr,imazapic, imazethapyr, imazaquin, pyrithiobac-sodium, bispyribac-sodium,thiencarbazone-methyl, azimsulfuron, cyclosulfamuron, chlorimuron-ethyl,metsulfuron-methyl, mesosulfuron-methyl, halosulfuron-methyl,nicosulfuron, orthosulfamuron, iodosulfuron-methyl-sodium, rimsulfuron,tribenuron-methyl, propyrisulfuron, ethoxysulfuron, foramsulfuron,primisulfuron-methyl, chlorsulfuron, flazasulfuron, sulfosulfuron,penoxsulam, pyroxsulam, florasulam and diclosulam.

Particularly preferred herbicides B from the group b2) that can be usedin combination with an isoxazolo[5,4-b]pyridine of the formula (I)according to the present invention are selected from imazamox, imazapyr,imazapic, imazethapyr, bispyribac-sodium, thiencarbazone-methyl,cyclosulfamuron, metsulfuron-methyl, mesosulfuron-methyl,halosulfuron-methyl, nicosulfuron, iodosulfuron-methyl-sodium,rimsulfuron, tribenuron-methyl, propyrisulfuron, foramsulfuron,penoxsulam, pyroxsulam and florasulam.

b3) from the group of the photosynthesis inhibitors:

ametryn, amicarbazone, atrazine, bentazone, bentazone-sodium, bromoxyniland its salts and esters, chloridazone, chlorotoluron, cyanazine,desmedipham, diquat-dibromide, diuron, fluometuron, hexazinone, ioxyniland its salts and esters, isoproturon, lenacil, linuron, metamitron,methabenzthiazuron, metribuzin, paraquat, paraquat-dichloride,phenmedipham, propanil, pyridate, simazine, terbutryn, terbuthylazineand thidiazuron.

More preferred herbicides B from the group b3) that can be used incombination with an isoxazolo[5,4-b]pyridine of the formula (I)according to the present invention are selected from paraquat,pentanochlor, propanil, bentazone, bromoxynil, phenmedipham, pyridate,atrazine, terbuthylazine, ametryne, metribuzin, hexazinone,amicarbazone, bromacil, chlorotoluron, diuron and isoproturon.

Particularly preferred herbicides B from the group b3) that can be usedin combination with an isoxazolo[5,4-b]pyridine of the formula (I)according to the present invention are selected from paraquat,bentazone, bromoxynil, atrazine, terbuthylazine, metribuzin,amicarbazone and chlorotoluron.

b4) from the group of the protoporphyrinogen-IX oxidase inhibitors:

acifluorfen-sodium, bencarbazone, benzfendizone, butafenacil,carfentrazone-ethyl, cinidon-ethyl, flufenpyr-ethyl, flumiclorac-pentyl,flumioxazin, fluoroglycofen-ethyl, fomesafen, lactofen, oxadiargyl,oxadiazon, oxyfluorfen, pentoxazone, pyraflufen-ethyl, saflufenacil,sulfentrazone, tiafenacil, ethyl[3-[2-chloro-4-fluoro-5-(1-methyl-6-trifluoromethyl-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-3-yl)phenoxy]-2-pyridyloxy]acetate(CAS 353292-31-6; S-3100),N-ethyl-3-(2,6-dichloro-4-trifluoromethylphenoxy)-5-methyl-1H-pyrazole-1-carboxamide(CAS 452098-92-9),N-tetrahydrofurfuryl-3-(2,6-dichloro-4-trifluoromethylphenoxy)-5-methyl-1H-pyrazole-1-carboxamide(CAS 915396-43-9),N-ethyl-3-(2-chloro-6-fluoro-4-trifluoromethylphenoxy)-5-methyl-1H-pyrazole-1-carboxamide(CAS 452099-05-7),N-tetrahydrofurfuryl-3-(2-chloro-6-fluoro-4-trifluoromethylphenoxy)-5-methyl-1H-pyrazole-1-carboxamide(CAS 452100-03-7),3-[7-fluoro-3-oxo-4-(prop-2-ynyl)-3,4-dihydro-2H-benzo[1,4]oxazin-6-yl]-1,5-dimethyl-6-thioxo-[1,3,5]triazinan-2,4-dione(CAS 451484-50-7),1,5-dimethyl-6-thioxo-3-(2,2,7-trifluoro-3-oxo-4-(prop-2-ynyl)-3,4-dihydro-2H-benzo[b][1,4]oxazin-6-yl)-1,3,5-triazinane-2,4-dione(CAS 1258836-72-4),2-(2,2,7-Trifluoro-3-oxo-4-prop-2-ynyl-3,4-dihydro-2H-benzo[1,4]oxazin-6-yl)-4,5,6,7-tetrahydro-isoindole-1,3-dione(CAS1300118-96-0);1-Methyl-6-trifluoromethyl-3-(2,2,7-trifluoro-3-oxo-4-prop-2-ynyl-3,4-dihydro-2H-benzo[1,4]oxazin-6-yl)-1H-pyrimidine-2,4-dione(CAS 1304113-05-0), and 3-[7-Chloro-5-fluoro-2-(trifluoromethyl)-1H-benzimidazol-4-yl]-1-methyl-6-(trifluoromethyl)-1H-pyrimidine-2,4-dione(CAS 212754-02-4);

More preferred herbicides B from the group b4) that can be used incombination with an isoxazolo[5,4-b]pyridine of the formula (I)according to the present invention are selected from acifluorfen-sodium,fomesafen, oxyfluorfen, flumioxazin, cinidon-ethyl, pyraclonil,oxadiargyl, oxadiazon, pentoxazone, saflufenacil,1,5-dimethyl-6-thioxo-3-(2,2,7-trifluoro-3-oxo-4-(prop-2-ynyl)-3,4-dihydro-2H-benzo[b][1,4]oxazin-6-yl)-1,3,5-triazinane-2,4-dione(CAS 1258836-72-4), carfentrazone-ethyl and sulfentrazone.

Particularly preferred herbicides B from the group b4) that can be usedin combination with an isoxazolo[5,4-b]pyridine of the formula (I)according to the present invention are selected from acifluorfen-sodium,fomesafen, flumioxazin, oxadiargyl, saflufenacil, trifludimoxazin,carfentrazone-ethyl and sulfentrazone.

b5) from the group of the bleacher herbicides:

aclonifen, amitrole, beflubutamid, benzobicyclon, bicyclopyrone,clomazone, diflufenican, fenquinotrione, flumeturon, flurochloridone,flurtamone, isoxaflutole, mesotrione, norflurazon, picolinafen,pyrasulfotole, pyrazolynate, sulcotrione, tefuryltrione, tembotrione,topramezone and4-(3-trifluoromethylphenoxy)-2-(4-trifluoromethylphenyl)pyrimidine (CAS180608-33-7);

More preferred herbicides B from the group b5) that can be used incombination with an isoxazolo[5,4-b]pyridine of the formula (I)according to the present invention are selected from aclonifen,pyrasulfotole, isoxaflutole, topramezone, benzobicyclon, bicyclopyrone,tembotrione, mesotrione, tefuryltrione, sulcotrione, clomazone,diflufenican and picolinafen.

Particularly preferred herbicides B from the group b5) that can be usedin combination with an isoxazolo[5,4-b]pyridine of the formula (I)according to the present invention are selected from pyrasulfotole,isoxaflutole, topramezone, benzobicyclon, bicyclopyrone, tembotrione,mesotrione, tefuryltrione, and picolinafen.

b6) from the group of the EPSP synthase inhibitors:

glyphosate, glyphosate-isopropylammonium, glyphosate-potassium andglyphosate-trimesium (sulfosate).

A more preferred herbicide B from the group b6) that can be used incombination with an isoxazolo[5,4-b]pyridine of the formula (I)according to the present invention is glyphosate.

b7) from the group of the glutamine synthase inhibitors:

glufosinate, glufosinate-P, glufosinate-ammonium.

A more preferred herbicide B from the group b7) that can be used incombination with an isoxazolo[5,4-b]pyridine of the formula (I)according to the present invention is glufosinate-ammonium.

b8) from the group of the DHP synthase inhibitors: asulam.

b9) from the group of the mitosis inhibitors:

chlorpropham, benfluralin, dithiopyr, ethalfluralin, oryzalin,pendimethalin, propyzamide (=pronamide), thiazopyr and trifluralin.

More preferred herbicides B from the group b9) that can be used incombination with an isoxazolo[5,4-b]pyridine of the formula (I)according to the present invention are selected from chlorpropham,propyzamide (=pronamide), pendimethalin, and trifluralin.

Particularly preferred herbicides B from the group b9) that can be usedin combination with an isoxazolo[5,4-b]pyridine of the formula (I)according to the present invention are selected from chlorpropham,propyzamide (=pronamide) and pendimethalin.

b10) from the group of the VLCFA inhibitors:

acetochlor, alachlor, anilofos, butachlor, cafenstrole, dimethenamid,dimethenamid-P, fentrazamide, flufenacet, mefenacet, metazachlor,metolachlor, S-metolachlor, naproanilide, napropamide, napropamide-M,pretilachlor, fenoxasulfone, ipfencarbazone, pyroxasulfone thenylchlorand isoxazoline-compounds of the formulae II.1, II.2, II.3, II.4, II.5,II.6, II.7, II.8 and II.9 as mentioned above.

More preferred herbicides B from the group b10) that can be used incombination with an isoxazolo[5,4-b]pyridine of the formula (I)according to the present invention are selected from alachlor,butachlor, cafenstrole, dimethenamid, flufenacet, ipfencarbazone,metazachlor, metolachlor, mefenacet, napropamide, pretilachlor andpyroxasulfone.

Particularly preferred herbicides B from the group b10) that can be usedin combination with an isoxazolo[5,4-b]pyridine of the formula (I)according to the present invention are selected from dimethenamid,flufenacet, metazachlor, metolachlor, pretilachlor and pyroxasulfone.

b11) from the group of the cellulose biosynthesis inhibitors:chlorthiamid, dichlobenil, flupoxam, indaziflam, isoxaben, triaziflamand 1-Cyclohexyl-5-pentafluorphenyloxy-1⁴-[1,2,4,6]thiatriazin-3-ylamine

More preferred herbicides B from the group b11) that can be used incombination with an isoxazolo[5,4-b]pyridine of the formula (I)according to the present invention are selected from dichlobenil,flupoxam, indaziflam, isoxaben and triaziflam.

Particularly preferred herbicides B from the group b11) that can be usedin combination with an isoxazolo[5,4-b]pyridine of the formula (I)according to the present invention are selected from indaziflam andisoxaben.

b13) from the group of the auxinic herbicides:

2,4-D and its salts and esters, aminocyclopyrachlor and its salts andesters, aminopyralid and its salts such asaminopyralid-dimethylammonium,aminopyralid-tris(2-hydroxypropyl)ammonium and its esters, clopyralidand its salts and esters, dicamba and its salts and esters,dichlorprop-P and its salts and esters, fluroxypyr-meptyl, halauxifenand its salts and esters (CAS 943832-60-8), e.g. halauxifen-methyl, MCPAand its salts and esters, MCPB and its salts and esters, mecoprop-P andits salts and esters, picloram and its salts and esters, quinclorac,quinmerac and triclopyr and its salts and esters,4-amino-3-chloro-6-(4-chloro-2-fluoro-3-methoxyphenyl)-5-fluoropyridine-2-carboxylicacid and its salts and esters, e.g. benzyl4-amino-3-chloro-6-(4-chloro-2-fluoro-3-methoxyphenyl)-5-fluoropyridine-2-carboxylate(CAS 1390661-72-9).

More preferred herbicides B from the group b13) that can be used incombination with an isoxazolo[5,4-b]pyridine of the formula (I)according to the present invention are selected from dicamba and itssalts and esters, halauxifen and its salts and esters,), e.g.halauxifen-methyl, 2,4-D and its salts and esters, MCPA and its saltsand esters, picloram and its salts and esters, aminopyralid and itssalts and esters, fluroxypyr, quinclorac and its salts and esters,quinmerac and its salts and esters and triclopyr and its salts andesters,4-amino-3-chloro-6-(4-chloro-2-fluoro-3-methoxyphenyl)-5-fluoropyridine-2-carboxylicacid and its salts and esters, e.g. benzyl4-amino-3-chloro-6-(4-chloro-2-fluoro-3-methoxyphenyl)-5-fluoropyridine-2-carboxylate(CAS 1390661-72-9).

Particularly preferred herbicides B from the group b13) that can be usedin combination with an isoxazolo[5,4-b]pyridine of the formula (I)according to the present invention are selected from dicamba and itssalts and esters, halauxifen and its salts and esters, e.g.halauxifen-methyl, 2,4-D and its salts and esters, MCPA and its saltsand esters, aminopyralid and its salts and esters, quinclorac and itssalts and esters and quinmerac and its salts and esters,4-amino-3-chloro-6-(4-chloro-2-fluoro-3-methoxyphenyl)-5-fluoropyridine-2-carboxylicacid and its salts and esters, e.g. benzyl4-amino-3-chloro-6-(4-chloro-2-fluoro-3-methoxyphenyl)-5-fluoropyridine-2-carboxylate(CAS 1390661-72-9).

b14) from the group of the auxin transport inhibitors: diflufenzopyr,diflufenzopyr-sodium and naptalam.

More preferred herbicides B from the group b14) that can be used incombination with an isoxazolo[5,4-b]pyridine of the formula (I)according to the present invention are selected from naptalam anddiflufenzopyr-sodium.

b15) from the group of the other herbicides: bromobutide, (1RS,2SR,4SR)-1, 4-epoxy-p-menth-2-yl2-methylbenzyl ether, cumyluron,cyclopyrimorate (CAS 499223-49-3) and its salts and esters, dalapon,difenzoquat, difenzoquat-metilsulfate, DSMA, dymron (=daimuron),indanofan, metam, methylbromide, MSMA, oxaziclomefone, pyributicarb, andtridiphane.

A more preferred herbicide B from the group b15) that can be used incombination with the an isoxazolo[5,4-b]pyridine of the formula (I)according to the present invention is(1RS,2SR,4SR)-1,4-epoxy-p-menth-2-yl2-methylbenzyl ether

In another embodiment of the present invention the compositionsaccording to the present invention comprise at least oneisoxazolo[5,4-b]pyridine of formula (I) and at least one safener C.

Safeners are chemical compounds which prevent or reduce damage on usefulplants without having a major impact on the herbicidal action of theherbicidal active components of the present compositions towardsunwanted plants. They can be applied either before sowings (e.g. on seedtreatments, shoots or seedlings) or in the pre-emergence application orpost-emergence application of the useful plant. The safeners and theisoxazolo[5,4-b]pyridine of formula (I) and/or the herbicides B can beapplied simultaneously or in succession.

Examples of preferred safeners C are benoxacor, cloquintocet,cyometrinil, cyprosulfamide, dichlormid, dicyclonon, dietholate,fenchlorazole, fenclorim, flurazole, fluxofenim, furilazole, isoxadifen,mefenpyr, mephenate, naphthalic anhydride, oxabetrinil,4-(dichloroacetyl)-1-oxa-4-azaspiro[4.5]decane (MON4660, CAS71526-07-3), 2,2,5-trimethyl-3-(dichloroacetyl)-1,3-oxazolidine(R-29148, CAS 52836-31-4),N-(2-Methoxybenzoyl)-4-[(methylaminocarbonyl)amino]benzenesulfonamide(CAS 129531-12-0), MG191 (2-dichloromethyl-2-methyl-1,3-dioxolane) ortheir salts and esters.

Especially preferred safeners C are benoxacor, cloquintocet,cyprosulfamide, dichlormid, fenchlorazole, fenclorim, flurazole,fluxofenim, furilazole, isoxadifen, mefenpyr, naphthalic anhydride,oxabetrinil, 4-(dichloroacetyl)-1-oxa-4-azaspiro[4.5]decane (MON4660,CAS 71526-07-3), 2,2,5-trimethyl-3-(dichloroacetyl)-1,3-oxazolidine(R-29148, CAS 52836-31-4) andN-(2-Methoxybenzoyl)-4-[(methylaminocarbonyl)amino]benzenesulfonamide(CAS 129531-12-0) or their salts and esters.

Particularly preferred safeners C are benoxacor, cloquintocet,cyprosulfamide, dichlormid, fenchlorazole, fenclorim, furilazole,isoxadifen, mefenpyr, naphtalic anhydride,4-(dichloroacetyl)-1-oxa-4-azaspiro[4.5]decane (MON4660, CAS71526-07-3), 2,2,5-trimethyl-3-(dichloroacetyl)-1,3-oxazolidine(R-29148, CAS 52836-31-4) andN-(2-Methoxybenzoyl)-4-[(methylaminocarbonyl)amino]benzenesulfonamide(CAS 129531-12-0) or their salts and esters.

The active compounds B of groups b1) to b15) and the active compounds Care known herbicides and safeners, see, for example, The Compendium ofPesticide Common Names (http://www.alanwood.net/pesticides/); FarmChemicals Handbook 2000 volume 86, Meister Publishing Company, 2000; B.Hock, C. Fedtke, R. R. Schmidt, Herbizide [Herbicides], Georg ThiemeVerlag, Stuttgart 1995; W. H. Ahrens, Herbicide Handbook, 7th edition,Weed Science Society of America, 1994; and K. K. Hatzios, HerbicideHandbook, Supplement for the 7th edition, Weed Science Society ofAmerica, 1998. 2,2,5-Trimethyl-3-(dichloroacetyl)-1,3-oxazolidine [CASNo. 52836-31-4] is also referred to as R-29148.4-(Dichloroacetyl)-1-oxa-4-azaspiro[4.5]decane [CAS No. 71526-07-3] isalso referred to as AD-67 and MON 4660.

The assignment of the active compounds to the respective mechanisms ofaction is based on current knowledge. If several mechanisms of actionapply to one active compound, this substance was only assigned to onemechanism of action.

Composition components B (herbicides B) and C (safeners) having acarboxyl group can be employed in the form of the acid, in the form ofan agriculturally suitable salt as mentioned above or else in the formof an agriculturally acceptable derivative in the compositions accordingto the invention.

In the case of dicamba, suitable salts include those, where thecounterion is an agri-culturally acceptable cation. For example,suitable salts of dicamba are dicamba-sodium, dicamba-potassium,dicamba-methylammonium, dicamba-dimethylammonium,dicamba-isopropylammonium, dicamba-diglycolamine, dicamba-olamine,dicamba-diolamine, dicamba-trolamine,dicamba-N,N-bis-(3-aminopropyl)methylamine anddicamba-diethylenetriamine. Examples of a suitable ester aredicamba-methyl and dicamba-butotyl.

Suitable salts of 2,4-D are 2,4-D-ammonium, 2,4-D-dimethylammonium,2,4-D-diethylammonium, 2,4-D-diethanolammonium (2,4-D-diolamine),2,4-D-triethanolammonium, 2,4-D-isopropylammonium,2,4-D-triisopropanolammonium, 2,4-D-heptylammonium,2,4-D-dodecylammonium, 2,4-D-tetradecylammonium, 2,4-D-triethylammonium,2,4-D-tris(2-hydroxypropyl)ammonium, 2,4-D-tris(isopropyl)ammonium,2,4-D-trolamine, 2,4-D-lithium, 2,4-D-sodium. Examples of suitableesters of 2,4-D are 2,4-D-butotyl, 2,4-D-2-butoxypropyl,2,4-D-3-butoxypropyl, 2,4-D-butyl, 2,4-D-ethyl, 2,4-D-ethylhexyl,2,4-D-isobutyl, 2,4-D-isooctyl, 2,4-D-isopropyl, 2,4-D-meptyl,2,4-D-methyl, 2,4-D-octyl, 2,4-D-pentyl, 2,4-D-propyl, 2,4-D-tefuryl andclacyfos.

Suitable salts of 2,4-DB are for example 2,4-DB-sodium, 2,4-DB-potassiumand 2,4-DB-dimethylammonium. Suitable esters of 2,4-DB are for example2,4-DB-butyl and 2,4-DB-isoctyl.

Suitable salts of dichlorprop are for example dichlorprop-sodium,dichlorprop-potassium and dichlorprop-dimethylammonium. Examples ofsuitable esters of dichlorprop are dichlorprop-butotyl anddichlorprop-isoctyl.

Suitable salts and esters of MCPA include MCPA-butotyl, MCPA-butyl,MCPA-dime-thylammonium, MCPA-diolamine, MCPA-ethyl, MCPA-thioethyl,MCPA-2-ethylhexyl, MCPA-isobutyl, MCPA-isoctyl, MCPA-isopropyl,MCPA-isopropylammonium, MCPA-methyl, MCPA-olamine, MCPA-potassium,MCPA-sodium and MCPA-trolamine.

A suitable salt of MCPB is MCPB sodium. A suitable ester of MCPB isMCPB-ethyl.

Suitable salts of clopyralid are clopyralid-potassium,clopyralid-olamine and clopyralid-tris-(2-hydroxypropyl)ammonium.Example of suitable esters of clopyralid is clopyralid-methyl.

Examples of a suitable ester of fluroxypyr are fluroxypyr-meptyl andfluroxypyr-2-butoxy-1-methylethyl, wherein fluroxypyr-meptyl ispreferred.

Suitable salts of picloram are picloram-dimethylammonium,picloram-potassium, picloram-triisopropanolammonium,picloram-triisopropylammonium and picloram-trolamine. A suitable esterof picloram is picloram-isoctyl.

A suitable salt of triclopyr is triclopyr-triethylammonium. Suitableesters of triclopyr are for example triclopyr-ethyl andtriclopyr-butotyl.

Suitable salts and esters of chloramben include chloramben-ammonium,chloramben-diolamine, chloramben-methyl, chloramben-methylammonium andchloramben-sodium. Suitable salts and esters of 2,3,6-TBA include2,3,6-TBA-dimethylammonium, 2,3,6-TBA-lithium, 2,3,6-TBA-potassium and2,3,6-TBA-sodium.

Suitable salts and esters of aminopyralid includeaminopyralid-potassium, aminopyralid-dimethylammonium, andaminopyralid-tris(2-hydroxypropyl)ammonium.

Suitable salts of glyphosate are for example glyphosate-ammonium,glyphosate-diammonium, glyphoste-dimethylammonium,glyphosate-isopropylammonium, glyphosate-potassium, glyphosate-sodium,glyphosate-trimesium as well as the ethanolamine and diethanolaminesalts, preferably glyphosate-diammonium, glyphosate-isopropylammoniumand glyphosate-trimesium (sulfosate).

A suitable salt of glufosinate is for example glufosinate-ammonium.

A suitable salt of glufosinate-P is for example glufosinate-P-ammonium.

Suitable salts and esters of bromoxynil are for examplebromoxynil-butyrate, bromoxynil-heptanoate, bromoxynil-octanoate,bromoxynil-potassium and bromoxynil-sodium.

Suitable salts and esters of ioxonil are for example ioxonil-octanoate,ioxonil-potassium and ioxonil-sodium.

Suitable salts and esters of mecoprop include mecoprop-butotyl,mecoprop-dimethylammonium, mecoprop-diolamine, mecoprop-ethadyl,mecoprop-2-ethylhexyl, mecoprop-isoctyl, mecoprop-methyl,mecoprop-potassium, mecoprop-sodium and mecoprop-trolamine.

Suitable salts of mecoprop-P are for example mecoprop-P-butotyl,mecoprop-P-dimethylammonium, mecoprop-P-2-ethylhexyl,mecoprop-P-isobutyl, mecoprop-P-potassium and mecoprop-P-sodium.

A suitable salt of diflufenzopyr is for example diflufenzopyr-sodium.

A suitable salt of naptalam is for example naptalam-sodium.

Suitable salts and esters of aminocyclopyrachlor are for exampleaminocyclopyrachlor-dimethylammonium, aminocyclopyrachlor-methyl,aminocyclopyrachlor-triisopropanolammonium, aminocyclopyrachlor-sodiumand aminocyclopyrachlor-potassium.

A suitable salt of quinclorac is for examplequinclorac-dimethylammonium.

A suitable salt of quinmerac is for example quinmerac-dimethylammonium.

A suitable salt of imazamox is for example imazamox-ammonium.

Suitable salts of imazapic are for example imazapic-ammonium andimazapic-isopropylammonium.

Suitable salts of imazapyr are for example imazapyr-ammonium andimazapyr-isopropylammonium.

A suitable salt of imazaquin is for example imazaquin-ammonium.

Suitable salts of imazethapyr are for example imazethapyr-ammonium andimazethapyr-isopropylammonium.

A suitable salt of topramezone is for example topramezone-sodium.

According to a preferred embodiment of the invention, the compositioncomprises as herbicidal active component B at least one, preferablyexactly one herbicide B.

According to another preferred embodiment of the invention, thecomposition comprises as herbicidal active component B at least two,preferably exactly two herbicides B different from each other.

According to another preferred embodiment of the invention, thecomposition comprises as herbicidal active component B at least three,preferably exactly three herbicides B different from each other.

According to another preferred embodiment of the invention, thecomposition comprises as safening component C at least one, preferablyexactly one safener.

According to another preferred embodiment of the invention, thecomposition comprises as component B at least one, preferably exactlyone herbicide B, and as component C at least one, preferably exactlyone, safener.

According to another preferred embodiment of the invention, thecomposition comprises as component B at least two, preferably exactlytwo, herbicides B different from each other, and as component C at leastone, preferably exactly one, safener.

According to another preferred embodiment of the invention, thecomposition comprises as component B at least three, preferably exactlythree, herbicides B different from each other, and as component C atleast one, preferably exactly one, safener.

According to another preferred embodiment of the invention, thecomposition comprises as component A at least one, preferably exactlyone isoxazolo[5,4-b]pyridine of formula (I), preferably of formula(I.1), (I.2) or (I.3), especially preferred the compound (I.1), and ascomponent B at least one, preferably exactly one, herbicide B.

According to another preferred embodiment of the invention, thecomposition comprises as component A at least one, preferably exactlyone isoxazolo[5,4-b]pyridine of formula (I), preferably of formula(I.1), (I.2) or (I.3), especially preferred the compound (I.1), and atleast two, preferably exactly two, herbicides B different from eachother.

According to another preferred embodiment of the invention, thecomposition comprises as component A at least one, preferably exactlyone isoxazolo[5,4-b]pyridine of formula (I), preferably of formula(I.1), (I.2) or (I.3), especially preferred the compound (I.1), and atleast three, preferably exactly three, herbicides B different from eachother.

According to another preferred embodiment of the invention, thecomposition comprises as component A at least one, preferably exactlyone isoxazolo[5,4-b]pyridine of formula (I), preferably of formula(I.1), (I.2) or (I.3), especially preferred the compound (I.1), and ascomponent C at least one, preferably exactly one, safener C.

According to another preferred embodiment of the invention, thecomposition comprises as component A at least one, preferably exactlyone isoxazolo[5,4-b]pyridine of formula (I), preferably of formula(I.1), (I.2) or (I.3), especially preferred the compound (I.1), ascomponent B at least one, preferably exactly one, herbicide B, and ascomponent C at least one, preferably exactly one safener C.

According to another preferred embodiment of the invention, thecomposition comprises as component A at least one, preferably exactlyone isoxazolo[5,4-b]pyridine of formula (I), preferably of formula(I.1), (I.2) or (I.3), especially preferred the compound (I.1), at leasttwo, preferably exactly two herbicides B different from each other, andas component C at least one, preferably exactly one, safener C.

According to another preferred embodiment of the invention, thecomposition comprises as component A at least one, preferably exactlyone isoxazolo[5,4-b]pyridine of formula (I), preferably of formula(I.1), (I.2) or (I.3), especially preferred the compound (I.1), at leastthree, preferably exactly three herbicides B different from each other,and as component C at least one, preferably exactly one, safener C.

According to another preferred embodiment of the invention, thecomposition comprises, in addition to an isoxazolo[5,4-b]pyridine offormula (I), especially an isoxazolo[5,4-b]pyridine from the groupconsisting of (I.1), (I.2) and (I.3), as component B at least one andespecially exactly one herbicide B from group b1), in particularselected from the group consisting of clodinafop-propargyl,cyhalofop-butyl, fluazifop-P-butyl, fenoxaprop-P-ethyl,haloxyfop-P-methyl, metamifop, propaquizafop, quizalofop-P-methyl,quizalofop-P-tefuryl, clethodim, cycloxydim, sethoxydim, profoxydim,tepraloxydim, tralkoxydim, pinoxaden, molinate and tri-allate.

According to another preferred embodiment of the invention, thecomposition comprises, in addition to an isoxazolo[5,4-b]pyridine offormula (I), especially an active compound from the group consisting of(I.1), (I.2) and (I.3), as component B at least one and especiallyexactly one herbicide B from group b2), in particular selected from thegroup consisting of imazamox, imazapyr, imazapic, imazethapyr,imazaquin, pyrithiobac-sodium, bispyribac-sodium, thiencarbazone-methyl,azimsulfuron, cyclosulfamuron, chlorimuron-ethyl, metsulfuron-methyl,mesosulfuron-methyl, halosulfuron-methyl, nicosulfuron, orthosulfamuron,iodosulfuron-methyl-sodium, rimsulfuron, tribenuron-methyl,propyrisulfuron, ethoxysulfuron, foramsulfuron, primisulfuron-methyl,chlorsulfuron, flazasulfuron, sulfosulfuron, penoxsulam, florasulam anddiclosulam.

According to another preferred embodiment of the invention, thecomposition comprises, in addition to an isoxazolo[5,4-b]pyridine offormula (I), especially an active compound from the group consisting of(I.1), (I.2) and (I.3), as component B at least one and especiallyexactly one herbicide B from group b3), in particular selected from thegroup consisting of paraquat, pentanochlor, propanil, bentazone,bromoxynil, phenmedipham, pyridate, atrazine, terbuthylazine, ametryne,metribuzin, hexazinone, amicarbazone, bromacil, chlorotoluron, diuronand isoproturon.

According to another preferred embodiment of the invention, thecomposition comprises, in addition to an isoxazolo[5,4-b]pyridine offormula (I), especially an active compound from the group consisting of(I.1), (I.2) and (I.3), as component B at least one and especiallyexactly one herbicide B from group b4), in particular selected from thegroup consisting of acifluorfen-sodium, fomesafen, oxyfluorfen,flumioxazin, cinidon-ethyl, pyraclonil, oxadiargyl, pentoxazone,saflufenacil, trifludimoxazin, carfentrazone-ethyl and sulfentrazone.

According to another preferred embodiment of the invention, thecomposition comprises, in addition to an isoxazolo[5,4-b]pyridine offormula (I), especially an active compound from the group consisting of(I.1), (I.2) and (I.3), as component B at least one and especiallyexactly one herbicide B from group b5), in particular selected from thegroup consisting of aclonifen, pyrasulfotole, isoxaflutole, topramezone,benzobicyclon, bicyclopyrone, tembotrione, mesotrione, tefuryltrione,sulcotrione, clomazone, diflufenican and picolinafen.

According to another preferred embodiment of the invention, thecomposition comprises, in addition to an isoxazolo[5,4-b]pyridine offormula (I), especially an active compound from the group consisting of(I.1), (I.2) and (I.3), as component B at least one and especiallyexactly one herbicide B from group b6), in particular glyphosate.

According to another preferred embodiment of the invention, thecomposition comprises, in addition to an isoxazolo[5,4-b]pyridine offormula (I), especially an active compound from the group consisting of(I.1), (I.2) and (I.3), as component B at least one and especiallyexactly one herbicide B from group b7), in particularglufosinate-ammonium.

According to another preferred embodiment of the invention, thecomposition comprises, in addition to an isoxazolo[5,4-b]pyridine offormula (I), especially an active compound from the group consisting of(I.1), (I.2) and (I.3), as component B at least one and especiallyexactly one herbicide B from group b9), in particular selected from thegroup consisting of chlorpropham, ethalfluralin, propyzamide(=pronamide), pendimethalin, oryzalin and trifluralin.

According to another preferred embodiment of the invention, thecomposition comprises, in addition to an isoxazolo[5,4-b]pyridine offormula (I), especially an active compound from the group consisting of(I.1), (I.2) and (I.3), as component B at least one and especiallyexactly one herbicide B from group b10), in particular selected from thegroup consisting of alachlor, butachlor, cafenstrole, dimethenamid,flufenacet, ipfencarbazone, metazachlor, metolachlor, mefenacet,napropamide, pretilachlor and pyroxasulfone.

Likewise, preference is given to compositions comprising in addition toan isoxazolo[5,4-b]pyridine of formula (I), especially an activecompound from the group consisting of (I.1), (I.2) and (I.3), ascomponent B at least one and especially exactly one herbicide B fromgroup b10), in particular selected from the group consisting ofisoxazoline compounds of the formulae II.1, II.2, II.3, II.4, II.5,II.6, II.7, II.8 and II.9, as defined above.

According to another preferred embodiment of the invention, thecomposition comprises, in addition to an isoxazolo[5,4-b]pyridine offormula (I), especially an active compound from the group consisting of(I.1), (I.2) and (I.3), as component B at least one and especiallyexactly one herbicide B from group b11), in particular selected from thegroup consisting of dichlobenil, flupoxam, indaziflam, isoxaben andtriaziflam.

According to another preferred embodiment of the invention, thecomposition comprises, in addition to an isoxazolo[5,4-b]pyridine offormula (I), especially an active compound from the group consisting of(I.1), (I.2) and (I.3), as component B at least one and especiallyexactly one herbicide B from group b13), in particular selected from thegroup consisting of dicamba and its salts and esters, 2,4-D and itssalts and esters, halauxifen and its salts and esters, e.g.halauxifen-methyl, MCPA, aminopyralid and its salts such asaminopyralid-dimethylammonium,aminopyralid-tris(2-hydroxypropyl)ammonium and its esters, fluroxypyrand its salts and esters, fluroxypyr-meptyl and its salts and esters andtriclopyr and its salts and esters,4-amino-3-chloro-6-(4-chloro-2-fluoro-3-methoxyphenyl)-5-fluoropyridine-2-carboxylicacid and its salts and esters, e.g. benzyl4-amino-3-chloro-6-(4-chloro-2-fluoro-3-methoxyphenyl)-5-fluoropyridine-2-carboxylate(CAS 1390661-72-9).

According to another preferred embodiment of the invention, thecomposition comprises, in addition to an isoxazolo[5,4-b]pyridine offormula (I), especially an active compound from the group consisting of(I.1), (I.2) and (I.3), as component B at least one and especiallyexactly one herbicide B from group b14), in particular selected from thegroup consisting of naptalam and diflufenzopyr-sodium.

According to another preferred embodiment of the invention, thecomposition comprises, in addition to an isoxazolo[5,4-b]pyridine offormula (I), especially an active compound from the group consisting of(I.1), (I.2) and (I.3), as component B at least one and especiallyexactly one herbicide B from group b15), in particular (1 RS,2SR,4SR)-1,4-epoxy-p-menth-2-yl2-methylbenzyl ether.

According to another preferred embodiment of the invention, thecomposition comprises, in addition to an isoxazolo[5,4-b]pyridine offormula (I), especially an active compound from the group consisting of(I.1), (I.2) and (I.3), at least one and especially exactly one safenerC, in particular selected from the group consisting of benoxacor,cloquintocet, cyprosulfamide, dichlormid, fenchlorazole, fenclorim,furilazole, isoxadifen, mefenpyr, naphtalic anhydride,4-(dichloroacetyl)-1-oxa-4-azaspiro[4.5]decane (MON4660, CAS71526-07-3), 2,2,5-trimethyl-3-(dichloroacetyl)-1,3-oxazolidine(R-29148, CAS 52836-31-4) andN-(2-Methoxybenzoyl)-4-[(methylaminocarbonyl)amino]benzenesulfonamide(CAS 129531-12-0).

Further preferred embodiments relate to ternary compositions whichcorrespond to the binary compositions mentioned above and additionallycomprise a safener C, in particular selected from the group consistingof benoxacor, cloquintocet, cyprosulfamide, dichlormid, fenchlorazole,fenclorim, furilazole, isoxadifen, mefenpyr,4-(dichloroacetyl)-1-oxa-4-azaspiro[4.5]decane (MON4660, CAS 71526-07-3)and 2,2,5-trimethyl-3-(dichloroacetyl)-1,3-oxazolidine (R-29148, CAS52836-31-4).

Here and below, the term “binary compositions” includes compositionscomprising one or more, for example 1, 2 or 3 isoxazolo[5,4-b]pyridinesof the formula (I) and either one or more, for example 1, 2 or 3,herbicides B or one or more safeners C.

Correspondingly, the term “ternary compositions” includes compositionscomprising one or more, for example 1, 2 or 3 isoxazolo[5,4-b]pyridinesof the formula (I), one or more, for example 1, 2 or 3, herbicides B andone or more, for example 1, 2 or 3, safeners C.

In binary compositions comprising at least one isoxazolo[5,4-b]pyridineof the formula (I) as component A and as component B at least oneherbicide B, the weight ratio of the active compounds A:B is generallyin the range of from 1:1000 to 1000:1, preferably in the range of from1:500 to 500:1, in particular in the range of from 1:250 to 250:1 andparticularly preferably in the range of from 1:75 to 75:1.

In binary compositions comprising at least one isoxazolo[5,4-b]pyridineof the formula (I) as component A and at least one safener C, the weightratio of the active compounds A:C is generally in the range of from1:1000 to 1000:1, preferably in the range of from 1:500 to 500:1, inparticular in the range of from 1:250 to 250:1 and particularlypreferably in the range of from 1:75 to 75:1.

In ternary compositions comprising at least one isoxazolo[5,4-b]pyridineof formula (I) as component A and as component B at least one herbicideB and at least one safener C, the relative proportions by weight of thecomponents A:B are generally in the range of from 1:1000 to 1000:1,preferably in the range of from 1:500 to 500:1, in particular in therange of from 1:250 to 250:1 and particularly preferably in the range offrom 1:75 to 75:1, the weight ratio of the components A:C is generallyin the range of from 1:1000 to 1000:1, preferably in the range of from1:500 to 500:1, in particular in the range of from 1:250 to 250:1 andparticularly preferably in the range of from 1:75 to 75:1, and theweight ratio of the components B:C is generally in the range of from1:1000 to 1000:1, preferably in the range of from 1:500 to 500:1, inparticular in the range of from 1:250 to 250:1 and particularlypreferably in the range of from 1:75 to 75:1. The weight ratio ofcomponents A+B to component C is preferably in the range of from 1:500to 500:1, in particular in the range of from 1:250 to 250:1 andparticularly preferably in the range of from 1:75 to 75:1.

Particularly preferred herbicides B are the herbicides B as definedabove; in particular the herbicides B.1 to B.200 listed below in tableB:

TABLE B Herbicide B B.1 clethodim B.2 clodinafop-propargyl B.3cycloxydim B.4 cyhalofop-butyl B.5 fenoxaprop-ethyl B.6fenoxaprop-P-ethyl B.7 metamifop B.8 pinoxaden B.9 profoxydim B.10sethoxydim B.11 tepraloxydim B.12 tralkoxydim B.13 esprocarb B.14ethofumesate B.15 molinate B.16 prosulfocarb B.17 thiobencarb B.18triallate B.19 bensulfuron-methyl B.20 bispyribac-sodium B.21cloransulam-methyl B.22 chlorsulfuron B.23 clorimuron B.24cyclosulfamuron B.25 diclosulam B.26 florasulam B.27 flumetsulam B.28flupyrsulfuron-methyl-sodium B.29 foramsulfuron B.30 imazamox B.31imazamox-ammonium B.32 imazapic B.33 imazapic-ammonium B.34imazapic-isopropylammonium B.35 imazapyr B.36 imazapyr-ammonium B.37imazapyr-isopropylammonium B.38 imazaquin B.39 imazaquin-ammonium B.40imazethapyr B.41 imazethapyr-ammonium B.42 imazethapyr-isopropylammonium B.43 imazosulfuron B.44 iodosulfuron-methyl-sodiumB.45 iofensulfuron B.46 iofensulfuron-sodium B.47 mesosulfuron-methylB.48 metazosulfuron B.49 metsulfuron-methyl B.50 metosulam B.51nicosulfuron B.52 penoxsulam B.53 propoxycarbazon-sodium B.54pyrazosulfuron-ethyl B.55 pyribenzoxim B.56 pyriftalid B.57 pyroxsulamB.58 propyrisulfuron B.59 rimsulfuron B.60 sulfosulfuron B.61thiencarbazone-methyl B.62 thifensulfuron-methyl B.63 tribenuron-methylB.64 tritosulfuron B.65 triafamone B.66 ametryne B.67 atrazine B.68bentazon B.69 bromoxynil B.70 bromoxynil-octanoate B.71bromoxynil-heptanoate B.72 bromoxynil-potassium B.73 diuron B.74fluometuron B.75 hexazinone B.76 isoproturon B.77 linuron B.78metamitron B.79 metribuzin B.80 propanil B.81 simazin B.82terbuthylazine B.83 terbutryn B.84 paraquat-dichloride B.85 acifluorfenB.86 butafenacil B.87 carfentrazone-ethyl B.88 flumioxazin B.89fomesafen B.90 oxadiargyl B.91 oxyfluorfen B.92 saflufenacil B.93sulfentrazone B.94 ethyl [3-[2-chloro-4-fluoro-5-(1-methyl-6-trifluoromethyl-2,4-di- oxo-1,2,3,4-tetrahydropyrimidin-3-yl)phenoxy]-2-pyridyl- oxy]acetate (CAS 353292-31-6) B.95trifludimoxazin B.96 benzobicyclon B.97 clomazone B.98 diflufenican B.99flurochloridone B.100 isoxaflutole B.101 mesotrione B.102 norflurazoneB.103 picolinafen B.104 sulcotrione B.105 tefuryltrione B.106tembotrione B.107 topramezone B.108 topramezone-sodium B.109bicyclopyrone B.110 amitrole B.111 fluometuron B.112 fenquinotrioneB.113 glyphosate B.114 glyphosate-ammonium B.115glyphosate-dimethylammonium B.116 glyphosate-isopropylammonium B.117glyphosate-trimesium (sulfosate) B.118 glyphosate-potassium B.119glufosinate B.120 glufosinate-ammonium B.121 glufosinate-P B.122glufosinate-P-ammonium B.123 pendimethalin B.124 trifluralin B.125acetochlor B.126 butachlor B.127 cafenstrole B.128 dimethenamid-P B.129fentrazamide B.130 flufenacet B.131 mefenacet B.132 metazachlor B.133metolachlor B.134 S-metolachlor B.135 pretilachlor B.136 fenoxasulfoneB.137 isoxaben B.138 ipfencarbazone B.139 pyroxasulfone B.140 2,4-DB.141 2,4-D-isobutyl B.142 2,4-D-dimethylammonium B.143 2,4-D-N,N,N-trimethylethanolammonium B.144 aminopyralid B.145 aminopyralid-methylB.146 aminopyralid-dimethyl- ammonium B.147 aminopyralid-tris(2-hydroxypropyl)ammonium B.148 clopyralid B.149 clopyralid-methyl B.150clopyralid-olamine B.151 dicamba B.152 dicamba-butotyl B.153dicamba-diglycolamine B.154 dicamba-dimethylammonium B.155dicamba-diolamine B.156 dicamba-isopropylammonium B.157dicamba-potassium B.158 dicamba-sodium B.159 dicamba-trolamine B.160dicamba-N,N-bis-(3- aminopropyl)methylamine B.161dicamba-diethylenetriamine B.162 fluroxypyr B.163 fluroxypyr-meptylB.164 MCPA B.165 MCPA-2-ethylhexyl B.166 MCPA-dimethylammonium B.167quinclorac B.168 quinclorac-dimethylammonium B.169 quinmerac B.170quinmerac-dimethylammonium B.171 aminocyclopyrachlor B.172aminocyclopyrachlor-potassium B.173 aminocyclopyrachlor-methyl B.174diflufenzopyr B.175 diflufenzopyr-sodium B.176 dymron B.177 indanofanB.178 indaziflam B.179 oxaziclomefone B.180 triaziflam B.181 II.1 B.182II.2 B.183 II.3 B.184 II.4 B.185 II.5 B.186 II.6 B.187 II.7 B.188 II.8B.189 II.9 B.190 chlorotoluron B.191 pyridate B.192 phenmedipham B.193(1RS,2SR,4SR)-1,4-epoxy-p- menth-2-yl 2-methylbenzyl ether B.194pyraflufen B.195 pyraflufen-ethyl B.196 tolpyralate B.197 halauxifenB.198 halauxifen-methyl B.199 4-amino-3-chloro-6-(4-chloro-2-fluoro-3-methoxyphenyl)-5- fluoropyridine-2-carboxylic acid B.200 benzyl4-amino-3-chloro-6-(4- chloro-2-fluoro-3- methoxyphenyl)-5-fluoropyridine-2-carboxylate (CAS 1390661-72-9)

Particularly preferred safeners C, which, as component C, areconstituent of the composition according to the invention are thesafeners C as defined above; in particular the safeners C.1 to C.17listed below in table C:

TABLE C Safener C C.1 benoxacor C.2 cloquintocet C.3 cloquintocet-mexylC.4 cyprosulfamide C.5 dichlormid C.6 fenchlorazole C.7fenchlorazole-ethyl C.8 fenclorim C.9 furilazole C.10 isoxadifen C.11isoxadifen-ethyl C.12 mefenpyr C.13 mefenpyr-diethyl C.14 naphtalic acidanhydride C.15 4-(dichloroacetyl)-1-oxa-4- azaspiro[4.5]decane (CAS71526-07-3) C.16 2,2,5-trimethyl-3-(dichloro- acetyl)-1,3-oxazolidine(CAS 52836-31-4) C.17 N-(2-Methoxybenzoyl)-4-[(methylaminocarbonyl)amino]benzenesulfonamide (CAS 129531-12-0)

The weight ratios of the individual components in the preferredcompositions mentioned below are within the limits given above, inparticular within the preferred limits.

Particularly preferred are the compositions mentioned below comprisingan isoxazolo[5,4-b]pyridine of formula I as defined and the substance(s)as defined in the respective row of table 1; especially preferredcomprising as only herbicidal active compounds anisoxazolo[5,4-b]pyridine of formula I as defined and the substance(s) asdefined in the respective row of table 1; most preferably comprising asonly active compounds an isoxazolo[5,4-b]pyridine of formula I asdefined and the substance(s) as defined in the respective row of table1.

Particularly preferred are compositions (composition no. 1.1 to 1.3617),comprising as component A an isoxazolo[5,4-b]pyridine of formula (I.1)and as component B the herbicide(s) B and/or the safener C as defined inthe respective row of table 1:

Table 1 (compositions 1.1 to 1.3617):

comp. no. herbicide B safener C 1.1 B.1 — 1.2 B.2 — 1.3 B.3 — 1.4 B.4 —1.5 B.5 — 1.6 B.6 — 1.7 B.7 — 1.8 B.8 — 1.9 B.9 — 1.10 B.10 — 1.11 B.11— 1.12 B.12 — 1.13 B.13 — 1.14 B.14 — 1.15 B.15 — 1.16 B.16 — 1.17 B.17— 1.18 B.18 — 1.19 B.19 — 1.20 B.20 — 1.21 B.21 — 1.22 B.22 — 1.23 B.23— 1.24 B.24 — 1.25 B.25 — 1.26 B.26 — 1.27 B.27 — 1.28 B.28 — 1.29 B.29— 1.30 B.30 — 1.31 B.31 — 1.32 B.32 — 1.33 B.33 — 1.34 B.34 — 1.35 B.35— 1.36 B.36 — 1.37 B.37 — 1.38 B.38 — 1.39 B.39 — 1.40 B.40 — 1.41 B.41— 1.42 B.42 — 1.43 B.43 — 1.44 B.44 — 1.45 B.45 — 1.46 B.46 — 1.47 B.47— 1.48 B.48 — 1.49 B.49 — 1.50 B.50 — 1.51 B.51 — 1.52 B.52 — 1.53 B.53— 1.54 B.54 — 1.55 B.55 — 1.56 B.56 — 1.57 B.57 — 1.58 B.58. — 1.59 B.59— 1.60 B.60 — 1.61 B.61 — 1.62 B.62 — 1.63 B.63 — 1.64 B.64 — 1.65 B.65— 1.66 B.66 — 1.67 B.67 — 1.68 B.68 — 1.69 B.69 — 1.70 B.70 — 1.71 B.71— 1.72 B.72 — 1.73 B.73 — 1.74 B.74 — 1.75 B.75 — 1.76 B.76 — 1.77 B.77— 1.78 B.78 — 1.79 B.79 — 1.80 B.80 — 1.81 B.81 — 1.82 B.82 — 1.83 B.83— 1.84 B.84 — 1.85 B.85 — 1.86 B.86 — 1.87 B.87 — 1.88 B.88 — 1.89 B.89— 1.90 B.90 — 1.91 B.91 — 1.92 B.92 — 1.93 B.93 — 1.94 B.94 — 1.95 B.95— 1.96 B.96 — 1.97 B.97 — 1.98 B.98 — 1.99 B.99 — 1.100 B.100 — 1.101B.101 — 1.102 B.102 — 1.103 B.103 — 1.104 B.104 — 1.105 B.105 — 1.106B.106 — 1.107 B.107 — 1.108 B.108 — 1.109 B.109 — 1.110 B.110 — 1.111B.111 — 1.112 B.112 — 1.113 B.113 — 1.114 B.114 — 1.115 B.115 — 1.116B.116 — 1.117 B.117 — 1.118 B.118 — 1.119 B.119 — 1.120 B.120 — 1.121B.121 — 1.122 B.122 — 1.123 B.123 — 1.124 B.124 — 1.125 B.125 — 1.126B.126 — 1.127 B.127 — 1.128 B.128 — 1.129 B.129 — 1.130 B.130 — 1.131B.131 — 1.132 B.132 — 1.133 B.133 — 1.134 B.134 — 1.135 B.135 — 1.136B.136 — 1.137 B.137 — 1.138 B.138 — 1.139 B.139 — 1.140 B.140 — 1.141B.141 — 1.142 B.142 — 1.143 B.143 — 1.144 B.144 — 1.145 B.145 — 1.146B.146 — 1.147 B.147 — 1.148 B.148 — 1.149 B.149 — 1.150 B.150 — 1.151B.151 — 1.152 B.152 — 1.153 B.153 — 1.154 B.154 — 1.155 B.155 — 1.156B.156 — 1.157 B.157 — 1.158 B.158 — 1.159 B.159 — 1.160 B.160 — 1.161B.161 — 1.162 B.162 — 1.163 B.163 — 1.164 B.164 — 1.165 B.165 — 1.166B.166 — 1.167 B.167 — 1.168 B.168 — 1.169 B.169 — 1.170 B.170 — 1.171B.171 — 1.172 B.172 — 1.173 B.173 — 1.174 B.174 — 1.175 B.175 — 1.176B.176 — 1.177 B.177 — 1.178 B.178 — 1.179 B.179 — 1.180 B.180 — 1.181B.181 — 1.182 B.182 — 1.183 B.183 — 1.184 B.184 — 1.185 B.185 — 1.186B.186 — 1.187 B.187 — 1.188 B.188 — 1.189 B.189 — 1.190 B.190 — 1.191B.191 — 1.192 B.192 — 1.193 B.193 — 1.194 B-194 — 1.195 B-195 — 1.196B-196 — 1.197 B-197 — 1.198 B-198 — 1.199 B-199 — 1.200 B-200 — 1.201B.1 C.1 1.202 B.2 C.1 1.203 B.3 C.1 1.204 B.4 C.1 1.205 B.5 C.1 1.206B.6 C.1 1.207 B.7 C.1 1.208 B.8 C.1 1.209 B.9 C.1 1.210 B.10 C.1 1.211B.11 C.1 1.212 B.12 C.1 1.213 B.13 C.1 1.214 B.14 C.1 1.215 B.15 C.11.216 B.16 C.1 1.217 B.17 C.1 1.218 B.18 C.1 1.219 B.19 C.1 1.220 B.20C.1 1.221 B.21 C.1 1.222 B.22 C.1 1.223 B.23 C.1 1.224 B.24 C.1 1.225B.25 C.1 1.226 B.26 C.1 1.227 B.27 C.1 1.228 B.28 C.1 1.229 B.29 C.11.230 B.30 C.1 1.231 B.31 C.1 1.232 B.32 C.1 1.233 B.33 C.1 1.234 B.34C.1 1.235 B.35 C.1 1.236 B.36 C.1 1.237 B.37 C.1 1.238 B.38 C.1 1.239B.39 C.1 1.240 B.40 C.1 1.241 B.41 C.1 1.242 B.42 C.1 1.243 B.43 C.11.244 B.44 C.1 1.245 B.45 C.1 1.246 B.46 C.1 1.247 B.47 C.1 1.248 B.48C.1 1.249 B.49 C.1 1.250 B.50 C.1 1.251 B.51 C.1 1.252 B.52 C.1 1.253B.53 C.1 1.254 B.54 C.1 1.255 B.55 C.1 1.256 B.56 C.1 1.257 B.57 C.11.258 B.58. C.1 1.259 B.59 C.1 1.260 B.60 C.1 1.261 B.61 C.1 1.262 B.62C.1 1.263 B.63 C.1 1.264 B.64 C.1 1.265 B.65 C.1 1.266 B.66 C.1 1.267B.67 C.1 1.268 B.68 C.1 1.269 B.69 C.1 1.270 B.70 C.1 1.271 B.71 C.11.272 B.72 C.1 1.273 B.73 C.1 1.274 B.74 C.1 1.275 B.75 C.1 1.276 B.76C.1 1.277 B.77 C.1 1.278 B.78 C.1 1.279 B.79 C.1 1.280 B.80 C.1 1.281B.81 C.1 1.282 B.82 C.1 1.283 B.83 C.1 1.284 B.84 C.1 1.285 B.85 C.11.286 B.86 C.1 1.287 B.87 C.1 1.288 B.88 C.1 1.289 B.89 C.1 1.290 B.90C.1 1.291 B.91 C.1 1.292 B.92 C.1 1.293 B.93 C.1 1.294 B.94 C.1 1.295B.95 C.1 1.296 B.96 C.1 1.297 B.97 C.1 1.298 B.98 C.1 1.299 B.99 C.11.300 B.100 C.1 1.301 B.101 C.1 1.302 B.102 C.1 1.303 B.103 C.1 1.304B.104 C.1 1.305 B.105 C.1 1.306 B.106 C.1 1.307 B.107 C.1 1.308 B.108C.1 1.309 B.109 C.1 1.310 B.110 C.1 1.311 B.111 C.1 1.312 B.112 C.11.313 B.113 C.1 1.314 B.114 C.1 1.315 B.115 C.1 1.316 B.116 C.1 1.317B.117 C.1 1.318 B.118 C.1 1.319 B.119 C.1 1.320 B.120 C.1 1.321 B.121C.1 1.322 B.122 C.1 1.323 B.123 C.1 1.324 B.124 C.1 1.325 B.125 C.11.326 B.126 C.1 1.327 B.127 C.1 1.328 B.128 C.1 1.329 B.129 C.1 1.330B.130 C.1 1.331 B.131 C.1 1.332 B.132 C.1 1.333 B.133 C.1 1.334 B.134C.1 1.335 B.135 C.1 1.336 B.136 C.1 1.337 B.137 C.1 1.338 B.138 C.11.339 B.139 C.1 1.340 B.140 C.1 1.341 B.141 C.1 1.342 B.142 C.1 1.343B.143 C.1 1.344 B.144 C.1 1.345 B.145 C.1 1.346 B.146 C.1 1.347 B.147C.1 1.348 B.148 C.1 1.349 B.149 C.1 1.350 B.150 C.1 1.351 B.151 C.11.352 B.152 C.1 1.353 B.153 C.1 1.354 B.154 C.1 1.355 B.155 C.1 1.356B.156 C.1 1.357 B.157 C.1 1.358 B.158 C.1 1.359 B.159 C.1 1.360 B.160C.1 1.361 B.161 C.1 1.362 B.162 C.1 1.363 B.163 C.1 1.364 B.164 C.11.365 B.165 C.1 1.366 B.166 C.1 1.367 B.167 C.1 1.368 B.168 C.1 1.369B.169 C.1 1.370 B.170 C.1 1.371 B.171 C.1 1.372 B.172 C.1 1.373 B.173C.1 1.374 B.174 C.1 1.375 B.175 C.1 1.376 B.176 C.1 1.377 B.177 C.11.378 B.178 C.1 1.379 B.179 C.1 1.380 B.180 C.1 1.381 B.181 C.1 1.382B.182 C.1 1.383 B.183 C.1 1.384 B.184 C.1 1.385 B.185 C.1 1.386 B.186C.1 1.387 B.187 C.1 1.388 B.188 C.1 1.389 B.189 C.1 1.390 B.190 C.11.391 B.191 C.1 1.392 B.192 C.1 1.393 B.193 C.1 1.394 B-194 C.1 1.395B-195 C.1 1.396 B-196 C.1 1.397 B-197 C.1 1.398 B-198 C.1 1.399 B-199C.1 1.400 B-200 C.1 1.401 B.1 C.2 1.402 B.2 C.2 1.403 B.3 C.2 1.404 B.4C.2 1.405 B.5 C.2 1.406 B.6 C.2 1.407 B.7 C.2 1.408 B.8 C.2 1.409 B.9C.2 1.410 B.10 C.2 1.411 B.11 C.2 1.412 B.12 C.2 1.413 B.13 C.2 1.414B.14 C.2 1.415 B.15 C.2 1.416 B.16 C.2 1.417 B.17 C.2 1.418 B.18 C.21.419 B.19 C.2 1.420 B.20 C.2 1.421 B.21 C.2 1.422 B.22 C.2 1.423 B.23C.2 1.424 B.24 C.2 1.425 B.25 C.2 1.426 B.26 C.2 1.427 B.27 C.2 1.428B.28 C.2 1.429 B.29 C.2 1.430 B.30 C.2 1.431 B.31 C.2 1.432 B.32 C.21.433 B.33 C.2 1.434 B.34 C.2 1.435 B.35 C.2 1.436 B.36 C.2 1.437 B.37C.2 1.438 B.38 C.2 1.439 B.39 C.2 1.440 B.40 C.2 1.441 B.41 C.2 1.442B.42 C.2 1.443 B.43 C.2 1.444 B.44 C.2 1.445 B.45 C.2 1.446 B.46 C.21.447 B.47 C.2 1.448 B.48 C.2 1.449 B.49 C.2 1.450 B.50 C.2 1.451 B.51C.2 1.452 B.52 C.2 1.453 B.53 C.2 1.454 B.54 C.2 1.455 B.55 C.2 1.456B.56 C.2 1.457 B.57 C.2 1.458 B.58. C.2 1.459 B.59 C.2 1.460 B.60 C.21.461 B.61 C.2 1.462 B.62 C.2 1.463 B.63 C.2 1.464 B.64 C.2 1.465 B.65C.2 1.466 B.66 C.2 1.467 B.67 C.2 1.468 B.68 C.2 1.469 B.69 C.2 1.470B.70 C.2 1.471 B.71 C.2 1.472 B.72 C.2 1.473 B.73 C.2 1.474 B.74 C.21.475 B.75 C.2 1.476 B.76 C.2 1.477 B.77 C.2 1.478 B.78 C.2 1.479 B.79C.2 1.480 B.80 C.2 1.481 B.81 C.2 1.482 B.82 C.2 1.483 B.83 C.2 1.484B.84 C.2 1.485 B.85 C.2 1.486 B.86 C.2 1.487 B.87 C.2 1.488 B.88 C.21.489 B.89 C.2 1.490 B.90 C.2 1.491 B.91 C.2 1.492 B.92 C.2 1.493 B.93C.2 1.494 B.94 C.2 1.495 B.95 C.2 1.496 B.96 C.2 1.497 B.97 C.2 1.498B.98 C.2 1.499 B.99 C.2 1.500 B.100 C.2 1.501 B.101 C.2 1.502 B.102 C.21.503 B.103 C.2 1.504 B.104 C.2 1.505 B.105 C.2 1.506 B.106 C.2 1.507B.107 C.2 1.508 B.108 C.2 1.509 B.109 C.2 1.510 B.110 C.2 1.511 B.111C.2 1.512 B.112 C.2 1.513 B.113 C.2 1.514 B.114 C.2 1.515 B.115 C.21.516 B.116 C.2 1.517 B.117 C.2 1.518 B.118 C.2 1.519 B.119 C.2 1.520B.120 C.2 1.521 B.121 C.2 1.522 B.122 C.2 1.523 B.123 C.2 1.524 B.124C.2 1.525 B.125 C.2 1.526 B.126 C.2 1.527 B.127 C.2 1.528 B.128 C.21.529 B.129 C.2 1.530 B.130 C.2 1.531 B.131 C.2 1.532 B.132 C.2 1.533B.133 C.2 1.534 B.134 C.2 1.535 B.135 C.2 1.536 B.136 C.2 1.537 B.137C.2 1.538 B.138 C.2 1.539 B.139 C.2 1.540 B.140 C.2 1.541 B.141 C.21.542 B.142 C.2 1.543 B.143 C.2 1.544 B.144 C.2 1.545 B.145 C.2 1.546B.146 C.2 1.547 B.147 C.2 1.548 B.148 C.2 1.549 B.149 C.2 1.550 B.150C.2 1.551 B.151 C.2 1.552 B.152 C.2 1.553 B.153 C.2 1.554 B.154 C.21.555 B.155 C.2 1.556 B.156 C.2 1.557 B.157 C.2 1.558 B.158 C.2 1.559B.159 C.2 1.560 B.160 C.2 1.561 B.161 C.2 1.562 B.162 C.2 1.563 B.163C.2 1.564 B.164 C.2 1.565 B.165 C.2 1.566 B.166 C.2 1.567 B.167 C.21.568 B.168 C.2 1.569 B.169 C.2 1.570 B.170 C.2 1.571 B.171 C.2 1.572B.172 C.2 1.573 B.173 C.2 1.574 B.174 C.2 1.575 B.175 C.2 1.576 B.176C.2 1.577 B.177 C.2 1.578 B.178 C.2 1.579 B.179 C.2 1.580 B.180 C.21.581 B.181 C.2 1.582 B.182 C.2 1.583 B.183 C.2 1.584 B.184 C.2 1.585B.185 C.2 1.586 B.186 C.2 1.587 B.187 C.2 1.588 B.188 C.2 1.589 B.189C.2 1.590 B.190 C.2 1.591 B.191 C.2 1.592 B.192 C.2 1.593 B.193 C.21.594 B-194 C.2 1.595 B-195 C.2 1.596 B-196 C.2 1.597 B-197 C.2 1.598B-198 C.2 1.599 B-199 C.2 1.600 B-200 C.2 1.601 B.1 C.3 1.602 B.2 C.31.603 B.3 C.3 1.604 B.4 C.3 1.605 B.5 C.3 1.606 B.6 C.3 1.607 B.7 C.31.608 B.8 C.3 1.609 B.9 C.3 1.610 B.10 C.3 1.611 B.11 C.3 1.612 B.12 C.31.613 B.13 C.3 1.614 B.14 C.3 1.615 B.15 C.3 1.616 B.16 C.3 1.617 B.17C.3 1.618 B.18 C.3 1.619 B.19 C.3 1.620 B.20 C.3 1.621 B.21 C.3 1.622B.22 C.3 1.623 B.23 C.3 1.624 B.24 C.3 1.625 B.25 C.3 1.626 B.26 C.31.627 B.27 C.3 1.628 B.28 C.3 1.629 B.29 C.3 1.630 B.30 C.3 1.631 B.31C.3 1.632 B.32 C.3 1.633 B.33 C.3 1.634 B.34 C.3 1.635 B.35 C.3 1.636B.36 C.3 1.637 B.37 C.3 1.638 B.38 C.3 1.639 B.39 C.3 1.640 B.40 C.31.641 B.41 C.3 1.642 B.42 C.3 1.643 B.43 C.3 1.644 B.44 C.3 1.645 B.45C.3 1.646 B.46 C.3 1.647 B.47 C.3 1.648 B.48 C.3 1.649 B.49 C.3 1.650B.50 C.3 1.651 B.51 C.3 1.652 B.52 C.3 1.653 B.53 C.3 1.654 B.54 C.31.655 B.55 C.3 1.656 B.56 C.3 1.657 B.57 C.3 1.658 B.58. C.3 1.659 B.59C.3 1.660 B.60 C.3 1.661 B.61 C.3 1.662 B.62 C.3 1.663 B.63 C.3 1.664B.64 C.3 1.665 B.65 C.3 1.666 B.66 C.3 1.667 B.67 C.3 1.668 B.68 C.31.669 B.69 C.3 1.670 B.70 C.3 1.671 B.71 C.3 1.672 B.72 C.3 1.673 B.73C.3 1.674 B.74 C.3 1.675 B.75 C.3 1.676 B.76 C.3 1.677 B.77 C.3 1.678B.78 C.3 1.679 B.79 C.3 1.680 B.80 C.3 1.681 B.81 C.3 1.682 B.82 C.31.683 B.83 C.3 1.684 B.84 C.3 1.685 B.85 C.3 1.686 B.86 C.3 1.687 B.87C.3 1.688 B.88 C.3 1.689 B.89 C.3 1.690 B.90 C.3 1.691 B.91 C.3 1.692B.92 C.3 1.693 B.93 C.3 1.694 B.94 C.3 1.695 B.95 C.3 1.696 B.96 C.31.697 B.97 C.3 1.698 B.98 C.3 1.699 B.99 C.3 1.700 B.100 C.3 1.701 B.101C.3 1.702 B.102 C.3 1.703 B.103 C.3 1.704 B.104 C.3 1.705 B.105 C.31.706 B.106 C.3 1.707 B.107 C.3 1.708 B.108 C.3 1.709 B.109 C.3 1.710B.110 C.3 1.711 B.111 C.3 1.712 B.112 C.3 1.713 B.113 C.3 1.714 B.114C.3 1.715 B.115 C.3 1.716 B.116 C.3 1.717 B.117 C.3 1.718 B.118 C.31.719 B.119 C.3 1.720 B.120 C.3 1.721 B.121 C.3 1.722 B.122 C.3 1.723B.123 C.3 1.724 B.124 C.3 1.725 B.125 C.3 1.726 B.126 C.3 1.727 B.127C.3 1.728 B.128 C.3 1.729 B.129 C.3 1.730 B.130 C.3 1.731 B.131 C.31.732 B.132 C.3 1.733 B.133 C.3 1.734 B.134 C.3 1.735 B.135 C.3 1.736B.136 C.3 1.737 B.137 C.3 1.738 B.138 C.3 1.739 B.139 C.3 1.740 B.140C.3 1.741 B.141 C.3 1.742 B.142 C.3 1.743 B.143 C.3 1.744 B.144 C.31.745 B.145 C.3 1.746 B.146 C.3 1.747 B.147 C.3 1.748 B.148 C.3 1.749B.149 C.3 1.750 B.150 C.3 1.751 B.151 C.3 1.752 B.152 C.3 1.753 B.153C.3 1.754 B.154 C.3 1.755 B.155 C.3 1.756 B.156 C.3 1.757 B.157 C.31.758 B.158 C.3 1.759 B.159 C.3 1.760 B.160 C.3 1.761 B.161 C.3 1.762B.162 C.3 1.763 B.163 C.3 1.764 B.164 C.3 1.765 B.165 C.3 1.766 B.166C.3 1.767 B.167 C.3 1.768 B.168 C.3 1.769 B.169 C.3 1.770 B.170 C.31.771 B.171 C.3 1.772 B.172 C.3 1.773 B.173 C.3 1.774 B.174 C.3 1.775B.175 C.3 1.776 B.176 C.3 1.777 B.177 C.3 1.778 B.178 C.3 1.779 B.179C.3 1.780 B.180 C.3 1.781 B.181 C.3 1.782 B.182 C.3 1.783 B.183 C.31.784 B.184 C.3 1.785 B.185 C.3 1.786 B.186 C.3 1.787 B.187 C.3 1.788B.188 C.3 1.789 B.189 C.3 1.790 B.190 C.3 1.791 B.191 C.3 1.792 B.192C.3 1.793 B.193 C.3 1.794 B-194 C.3 1.795 B-195 C.3 1.796 B-196 C.31.797 B-197 C.3 1.798 B-198 C.3 1.799 B-199 C.3 1.800 B-200 C.3 1.801B.1 C.4 1.802 B.2 C.4 1.803 B.3 C.4 1.804 B.4 C.4 1.805 B.5 C.4 1.806B.6 C.4 1.807 B.7 C.4 1.808 B.8 C.4 1.809 B.9 C.4 1.810 B.10 C.4 1.811B.11 C.4 1.812 B.12 C.4 1.813 B.13 C.4 1.814 B.14 C.4 1.815 B.15 C.41.816 B.16 C.4 1.817 B.17 C.4 1.818 B.18 C.4 1.819 B.19 C.4 1.820 B.20C.4 1.821 B.21 C.4 1.822 B.22 C.4 1.823 B.23 C.4 1.824 B.24 C.4 1.825B.25 C.4 1.826 B.26 C.4 1.827 B.27 C.4 1.828 B.28 C.4 1.829 B.29 C.41.830 B.30 C.4 1.831 B.31 C.4 1.832 B.32 C.4 1.833 B.33 C.4 1.834 B.34C.4 1.835 B.35 C.4 1.836 B.36 C.4 1.837 B.37 C.4 1.838 B.38 C.4 1.839B.39 C.4 1.840 B.40 C.4 1.841 B.41 C.4 1.842 B.42 C.4 1.843 B.43 C.41.844 B.44 C.4 1.845 B.45 C.4 1.846 B.46 C.4 1.847 B.47 C.4 1.848 B.48C.4 1.849 B.49 C.4 1.850 B.50 C.4 1.851 B.51 C.4 1.852 B.52 C.4 1.853B.53 C.4 1.854 B.54 C.4 1.855 B.55 C.4 1.856 B.56 C.4 1.857 B.57 C.41.858 B.58. C.4 1.859 B.59 C.4 1.860 B.60 C.4 1.861 B.61 C.4 1.862 B.62C.4 1.863 B.63 C.4 1.864 B.64 C.4 1.865 B.65 C.4 1.866 B.66 C.4 1.867B.67 C.4 1.868 B.68 C.4 1.869 B.69 C.4 1.870 B.70 C.4 1.871 B.71 C.41.872 B.72 C.4 1.873 B.73 C.4 1.874 B.74 C.4 1.875 B.75 C.4 1.876 B.76C.4 1.877 B.77 C.4 1.878 B.78 C.4 1.879 B.79 C.4 1.880 B.80 C.4 1.881B.81 C.4 1.882 B.82 C.4 1.883 B.83 C.4 1.884 B.84 C.4 1.885 B.85 C.41.886 B.86 C.4 1.887 B.87 C.4 1.888 B.88 C.4 1.889 B.89 C.4 1.890 B.90C.4 1.891 B.91 C.4 1.892 B.92 C.4 1.893 B.93 C.4 1.894 B.94 C.4 1.895B.95 C.4 1.896 B.96 C.4 1.897 B.97 C.4 1.898 B.98 C.4 1.899 B.99 C.41.900 B.100 C.4 1.901 B.101 C.4 1.902 B.102 C.4 1.903 B.103 C.4 1.904B.104 C.4 1.905 B.105 C.4 1.906 B.106 C.4 1.907 B.107 C.4 1.908 B.108C.4 1.909 B.109 C.4 1.910 B.110 C.4 1.911 B.111 C.4 1.912 B.112 C.41.913 B.113 C.4 1.914 B.114 C.4 1.915 B.115 C.4 1.916 B.116 C.4 1.917B.117 C.4 1.918 B.118 C.4 1.919 B.119 C.4 1.920 B.120 C.4 1.921 B.121C.4 1.922 B.122 C.4 1.923 B.123 C.4 1.924 B.124 C.4 1.925 B.125 C.41.926 B.126 C.4 1.927 B.127 C.4 1.928 B.128 C.4 1.929 B.129 C.4 1.930B.130 C.4 1.931 B.131 C.4 1.932 B.132 C.4 1.933 B.133 C.4 1.934 B.134C.4 1.935 B.135 C.4 1.936 B.136 C.4 1.937 B.137 C.4 1.938 B.138 C.41.939 B.139 C.4 1.940 B.140 C.4 1.941 B.141 C.4 1.942 B.142 C.4 1.943B.143 C.4 1.944 B.144 C.4 1.945 B.145 C.4 1.946 B.146 C.4 1.947 B.147C.4 1.948 B.148 C.4 1.949 B.149 C.4 1.950 B.150 C.4 1.951 B.151 C.41.952 B.152 C.4 1.953 B.153 C.4 1.954 B.154 C.4 1.955 B.155 C.4 1.956B.156 C.4 1.957 B.157 C.4 1.958 B.158 C.4 1.959 B.159 C.4 1.960 B.160C.4 1.961 B.161 C.4 1.962 B.162 C.4 1.963 B.163 C.4 1.964 B.164 C.41.965 B.165 C.4 1.966 B.166 C.4 1.967 B.167 C.4 1.968 B.168 C.4 1.969B.169 C.4 1.970 B.170 C.4 1.971 B.171 C.4 1.972 B.172 C.4 1.973 B.173C.4 1.974 B.174 C.4 1.975 B.175 C.4 1.976 B.176 C.4 1.977 B.177 C.41.978 B.178 C.4 1.979 B.179 C.4 1.980 B.180 C.4 1.981 B.181 C.4 1.982B.182 C.4 1.983 B.183 C.4 1.984 B.184 C.4 1.985 B.185 C.4 1.986 B.186C.4 1.987 B.187 C.4 1.988 B.188 C.4 1.989 B.189 C.4 1.990 B.190 C.41.991 B.191 C.4 1.992 B.192 C.4 1.993 B.193 C.4 1.994 B-194 C.4 1.995B-195 C.4 1.996 B-196 C.4 1.997 B-197 C.4 1.998 B-198 C.4 1.999 B-199C.4 1.1000 B-200 C.4 1.1001 B.1 C.5 1.1002 B.2 C.5 1.1003 B.3 C.5 1.1004B.4 C.5 1.1005 B.5 C.5 1.1006 B.6 C.5 1.1007 B.7 C.5 1.1008 B.8 C.51.1009 B.9 C.5 1.1010 B.10 C.5 1.1011 B.11 C.5 1.1012 B.12 C.5 1.1013B.13 C.5 1.1014 B.14 C.5 1.1015 B.15 C.5 1.1016 B.16 C.5 1.1017 B.17 C.51.1018 B.18 C.5 1.1019 B.19 C.5 1.1020 B.20 C.5 1.1021 B.21 C.5 1.1022B.22 C.5 1.1023 B.23 C.5 1.1024 B.24 C.5 1.1025 B.25 C.5 1.1026 B.26 C.51.1027 B.27 C.5 1.1028 B.28 C.5 1.1029 B.29 C.5 1.1030 B.30 C.5 1.1031B.31 C.5 1.1032 B.32 C.5 1.1033 B.33 C.5 1.1034 B.34 C.5 1.1035 B.35 C.51.1036 B.36 C.5 1.1037 B.37 C.5 1.1038 B.38 C.5 1.1039 B.39 C.5 1.1040B.40 C.5 1.1041 B.41 C.5 1.1042 B.42 C.5 1.1043 B.43 C.5 1.1044 B.44 C.51.1045 B.45 C.5 1.1046 B.46 C.5 1.1047 B.47 C.5 1.1048 B.48 C.5 1.1049B.49 C.5 1.1050 B.50 C.5 1.1051 B.51 C.5 1.1052 B.52 C.5 1.1053 B.53 C.51.1054 B.54 C.5 1.1055 B.55 C.5 1.1056 B.56 C.5 1.1057 B.57 C.5 1.1058B.58. C.5 1.1059 B.59 C.5 1.1060 B.60 C.5 1.1061 B.61 C.5 1.1062 B.62C.5 1.1063 B.63 C.5 1.1064 B.64 C.5 1.1065 B.65 C.5 1.1066 B.66 C.51.1067 B.67 C.5 1.1068 B.68 C.5 1.1069 B.69 C.5 1.1070 B.70 C.5 1.1071B.71 C.5 1.1072 B.72 C.5 1.1073 B.73 C.5 1.1074 B.74 C.5 1.1075 B.75 C.51.1076 B.76 C.5 1.1077 B.77 C.5 1.1078 B.78 C.5 1.1079 B.79 C.5 1.1080B.80 C.5 1.1081 B.81 C.5 1.1082 B.82 C.5 1.1083 B.83 C.5 1.1084 B.84 C.51.1085 B.85 C.5 1.1086 B.86 C.5 1.1087 B.87 C.5 1.1088 B.88 C.5 1.1089B.89 C.5 1.1090 B.90 C.5 1.1091 B.91 C.5 1.1092 B.92 C.5 1.1093 B.93 C.51.1094 B.94 C.5 1.1095 B.95 C.5 1.1096 B.96 C.5 1.1097 B.97 C.5 1.1098B.98 C.5 1.1099 B.99 C.5 1.1100 B.100 C.5 1.1101 B.101 C.5 1.1102 B.102C.5 1.1103 B.103 C.5 1.1104 B.104 C.5 1.1105 B.105 C.5 1.1106 B.106 C.51.1107 B.107 C.5 1.1108 B.108 C.5 1.1109 B.109 C.5 1.1110 B.110 C.51.1111 B.111 C.5 1.1112 B.112 C.5 1.1113 B.113 C.5 1.1114 B.114 C.51.1115 B.115 C.5 1.1116 B.116 C.5 1.1117 B.117 C.5 1.1118 B.118 C.51.1119 B.119 C.5 1.1120 B.120 C.5 1.1121 B.121 C.5 1.1122 B.122 C.51.1123 B.123 C.5 1.1124 B.124 C.5 1.1125 B.125 C.5 1.1126 B.126 C.51.1127 B.127 C.5 1.1128 B.128 C.5 1.1129 B.129 C.5 1.1130 B.130 C.51.1131 B.131 C.5 1.1132 B.132 C.5 1.1133 B.133 C.5 1.1134 B.134 C.51.1135 B.135 C.5 1.1136 B.136 C.5 1.1137 B.137 C.5 1.1138 B.138 C.51.1139 B.139 C.5 1.1140 B.140 C.5 1.1141 B.141 C.5 1.1142 B.142 C.51.1143 B.143 C.5 1.1144 B.144 C.5 1.1145 B.145 C.5 1.1146 B.146 C.51.1147 B.147 C.5 1.1148 B.148 C.5 1.1149 B.149 C.5 1.1150 B.150 C.51.1151 B.151 C.5 1.1152 B.152 C.5 1.1153 B.153 C.5 1.1154 B.154 C.51.1155 B.155 C.5 1.1156 B.156 C.5 1.1157 B.157 C.5 1.1158 B.158 C.51.1159 B.159 C.5 1.1160 B.160 C.5 1.1161 B.161 C.5 1.1162 B.162 C.51.1163 B.163 C.5 1.1164 B.164 C.5 1.1165 B.165 C.5 1.1166 B.166 C.51.1167 B.167 C.5 1.1168 B.168 C.5 1.1169 B.169 C.5 1.1170 B.170 C.51.1171 B.171 C.5 1.1172 B.172 C.5 1.1173 B.173 C.5 1.1174 B.174 C.51.1175 B.175 C.5 1.1176 B.176 C.5 1.1177 B.177 C.5 1.1178 B.178 C.51.1179 B.179 C.5 1.1180 B.180 C.5 1.1181 B.181 C.5 1.1182 B.182 C.51.1183 B.183 C.5 1.1184 B.184 C.5 1.1185 B.185 C.5 1.1186 B.186 C.51.1187 B.187 C.5 1.1188 B.188 C.5 1.1189 B.189 C.5 1.1190 B.190 C.51.1191 B.191 C.5 1.1192 B.192 C.5 1.1193 B.193 C.5 1.1194 B-194 C.51.1195 B-195 C.5 1.1196 B-196 C.5 1.1197 B-197 C.5 1.1198 B-198 C.51.1199 B-199 C.5 1.1200 B-200 C.5 1.1201 B.1 C.6 1.1202 B.2 C.6 1.1203B.3 C.6 1.1204 B.4 C.6 1.1205 B.5 C.6 1.1206 B.6 C.6 1.1207 B.7 C.61.1208 B.8 C.6 1.1209 B.9 C.6 1.1210 B.10 C.6 1.1211 B.11 C.6 1.1212B.12 C.6 1.1213 B.13 C.6 1.1214 B.14 C.6 1.1215 B.15 C.6 1.1216 B.16 C.61.1217 B.17 C.6 1.1218 B.18 C.6 1.1219 B.19 C.6 1.1220 B.20 C.6 1.1221B.21 C.6 1.1222 B.22 C.6 1.1223 B.23 C.6 1.1224 B.24 C.6 1.1225 B.25 C.61.1226 B.26 C.6 1.1227 B.27 C.6 1.1228 B.28 C.6 1.1229 B.29 C.6 1.1230B.30 C.6 1.1231 B.31 C.6 1.1232 B.32 C.6 1.1233 B.33 C.6 1.1234 B.34 C.61.1235 B.35 C.6 1.1236 B.36 C.6 1.1237 B.37 C.6 1.1238 B.38 C.6 1.1239B.39 C.6 1.1240 B.40 C.6 1.1241 B.41 C.6 1.1242 B.42 C.6 1.1243 B.43 C.61.1244 B.44 C.6 1.1245 B.45 C.6 1.1246 B.46 C.6 1.1247 B.47 C.6 1.1248B.48 C.6 1.1249 B.49 C.6 1.1250 B.50 C.6 1.1251 B.51 C.6 1.1252 B.52 C.61.1253 B.53 C.6 1.1254 B.54 C.6 1.1255 B.55 C.6 1.1256 B.56 C.6 1.1257B.57 C.6 1.1258 B.58. C.6 1.1259 B.59 C.6 1.1260 B.60 C.6 1.1261 B.61C.6 1.1262 B.62 C.6 1.1263 B.63 C.6 1.1264 B.64 C.6 1.1265 B.65 C.61.1266 B.66 C.6 1.1267 B.67 C.6 1.1268 B.68 C.6 1.1269 B.69 C.6 1.1270B.70 C.6 1.1271 B.71 C.6 1.1272 B.72 C.6 1.1273 B.73 C.6 1.1274 B.74 C.61.1275 B.75 C.6 1.1276 B.76 C.6 1.1277 B.77 C.6 1.1278 B.78 C.6 1.1279B.79 C.6 1.1280 B.80 C.6 1.1281 B.81 C.6 1.1282 B.82 C.6 1.1283 B.83 C.61.1284 B.84 C.6 1.1285 B.85 C.6 1.1286 B.86 C.6 1.1287 B.87 C.6 1.1288B.88 C.6 1.1289 B.89 C.6 1.1290 B.90 C.6 1.1291 B.91 C.6 1.1292 B.92 C.61.1293 B.93 C.6 1.1294 B.94 C.6 1.1295 B.95 C.6 1.1296 B.96 C.6 1.1297B.97 C.6 1.1298 B.98 C.6 1.1299 B.99 C.6 1.1300 B.100 C.6 1.1301 B.101C.6 1.1302 B.102 C.6 1.1303 B.103 C.6 1.1304 B.104 C.6 1.1305 B.105 C.61.1306 B.106 C.6 1.1307 B.107 C.6 1.1308 B.108 C.6 1.1309 B.109 C.61.1310 B.110 C.6 1.1311 B.111 C.6 1.1312 B.112 C.6 1.1313 B.113 C.61.1314 B.114 C.6 1.1315 B.115 C.6 1.1316 B.116 C.6 1.1317 B.117 C.61.1318 B.118 C.6 1.1319 B.119 C.6 1.1320 B.120 C.6 1.1321 B.121 C.61.1322 B.122 C.6 1.1323 B.123 C.6 1.1324 B.124 C.6 1.1325 B.125 C.61.1326 B.126 C.6 1.1327 B.127 C.6 1.1328 B.128 C.6 1.1329 B.129 C.61.1330 B.130 C.6 1.1331 B.131 C.6 1.1332 B.132 C.6 1.1333 B.133 C.61.1334 B.134 C.6 1.1335 B.135 C.6 1.1336 B.136 C.6 1.1337 B.137 C.61.1338 B.138 C.6 1.1339 B.139 C.6 1.1340 B.140 C.6 1.1341 B.141 C.61.1342 B.142 C.6 1.1343 B.143 C.6 1.1344 B.144 C.6 1.1345 B.145 C.61.1346 B.146 C.6 1.1347 B.147 C.6 1.1348 B.148 C.6 1.1349 B.149 C.61.1350 B.150 C.6 1.1351 B.151 C.6 1.1352 B.152 C.6 1.1353 B.153 C.61.1354 B.154 C.6 1.1355 B.155 C.6 1.1356 B.156 C.6 1.1357 B.157 C.61.1358 B.158 C.6 1.1359 B.159 C.6 1.1360 B.160 C.6 1.1361 B.161 C.61.1362 B.162 C.6 1.1363 B.163 C.6 1.1364 B.164 C.6 1.1365 B.165 C.61.1366 B.166 C.6 1.1367 B.167 C.6 1.1368 B.168 C.6 1.1369 B.169 C.61.1370 B.170 C.6 1.1371 B.171 C.6 1.1372 B.172 C.6 1.1373 B.173 C.61.1374 B.174 C.6 1.1375 B.175 C.6 1.1376 B.176 C.6 1.1377 B.177 C.61.1378 B.178 C.6 1.1379 B.179 C.6 1.1380 B.180 C.6 1.1381 B.181 C.61.1382 B.182 C.6 1.1383 B.183 C.6 1.1384 B.184 C.6 1.1385 B.185 C.61.1386 B.186 C.6 1.1387 B.187 C.6 1.1388 B.188 C.6 1.1389 B.189 C.61.1390 B.190 C.6 1.1391 B.191 C.6 1.1392 B.192 C.6 1.1393 B.193 C.61.1394 B-194 C.6 1.1395 B-195 C.6 1.1396 B-196 C.6 1.1397 B-197 C.61.1398 B-198 C.6 1.1399 B-199 C.6 1.1400 B-200 C.6 1.1401 B.1 C.7 1.1402B.2 C.7 1.1403 B.3 C.7 1.1404 B.4 C.7 1.1405 B.5 C.7 1.1406 B.6 C.71.1407 B.7 C.7 1.1408 B.8 C.7 1.1409 B.9 C.7 1.1410 B.10 C.7 1.1411 B.11C.7 1.1412 B.12 C.7 1.1413 B.13 C.7 1.1414 B.14 C.7 1.1415 B.15 C.71.1416 B.16 C.7 1.1417 B.17 C.7 1.1418 B.18 C.7 1.1419 B.19 C.7 1.1420B.20 C.7 1.1421 B.21 C.7 1.1422 B.22 C.7 1.1423 B.23 C.7 1.1424 B.24 C.71.1425 B.25 C.7 1.1426 B.26 C.7 1.1427 B.27 C.7 1.1428 B.28 C.7 1.1429B.29 C.7 1.1430 B.30 C.7 1.1431 B.31 C.7 1.1432 B.32 C.7 1.1433 B.33 C.71.1434 B.34 C.7 1.1435 B.35 C.7 1.1436 B.36 C.7 1.1437 B.37 C.7 1.1438B.38 C.7 1.1439 B.39 C.7 1.1440 B.40 C.7 1.1441 B.41 C.7 1.1442 B.42 C.71.1443 B.43 C.7 1.1444 B.44 C.7 1.1445 B.45 C.7 1.1446 B.46 C.7 1.1447B.47 C.7 1.1448 B.48 C.7 1.1449 B.49 C.7 1.1450 B.50 C.7 1.1451 B.51 C.71.1452 B.52 C.7 1.1453 B.53 C.7 1.1454 B.54 C.7 1.1455 B.55 C.7 1.1456B.56 C.7 1.1457 B.57 C.7 1.1458 B.58. C.7 1.1459 B.59 C.7 1.1460 B.60C.7 1.1461 B.61 C.7 1.1462 B.62 C.7 1.1463 B.63 C.7 1.1464 B.64 C.71.1465 B.65 C.7 1.1466 B.66 C.7 1.1467 B.67 C.7 1.1468 B.68 C.7 1.1469B.69 C.7 1.1470 B.70 C.7 1.1471 B.71 C.7 1.1472 B.72 C.7 1.1473 B.73 C.71.1474 B.74 C.7 1.1475 B.75 C.7 1.1476 B.76 C.7 1.1477 B.77 C.7 1.1478B.78 C.7 1.1479 B.79 C.7 1.1480 B.80 C.7 1.1481 B.81 C.7 1.1482 B.82 C.71.1483 B.83 C.7 1.1484 B.84 C.7 1.1485 B.85 C.7 1.1486 B.86 C.7 1.1487B.87 C.7 1.1488 B.88 C.7 1.1489 B.89 C.7 1.1490 B.90 C.7 1.1491 B.91 C.71.1492 B.92 C.7 1.1493 B.93 C.7 1.1494 B.94 C.7 1.1495 B.95 C.7 1.1496B.96 C.7 1.1497 B.97 C.7 1.1498 B.98 C.7 1.1499 B.99 C.7 1.1500 B.100C.7 1.1501 B.101 C.7 1.1502 B.102 C.7 1.1503 B.103 C.7 1.1504 B.104 C.71.1505 B.105 C.7 1.1506 B.106 C.7 1.1507 B.107 C.7 1.1508 B.108 C.71.1509 B.109 C.7 1.1510 B.110 C.7 1.1511 B.111 C.7 1.1512 B.112 C.71.1513 B.113 C.7 1.1514 B.114 C.7 1.1515 B.115 C.7 1.1516 B.116 C.71.1517 B.117 C.7 1.1518 B.118 C.7 1.1519 B.119 C.7 1.1520 B.120 C.71.1521 B.121 C.7 1.1522 B.122 C.7 1.1523 B.123 C.7 1.1524 B.124 C.71.1525 B.125 C.7 1.1526 B.126 C.7 1.1527 B.127 C.7 1.1528 B.128 C.71.1529 B.129 C.7 1.1530 B.130 C.7 1.1531 B.131 C.7 1.1532 B.132 C.71.1533 B.133 C.7 1.1534 B.134 C.7 1.1535 B.135 C.7 1.1536 B.136 C.71.1537 B.137 C.7 1.1538 B.138 C.7 1.1539 B.139 C.7 1.1540 B.140 C.71.1541 B.141 C.7 1.1542 B.142 C.7 1.1543 B.143 C.7 1.1544 B.144 C.71.1545 B.145 C.7 1.1546 B.146 C.7 1.1547 B.147 C.7 1.1548 B.148 C.71.1549 B.149 C.7 1.1550 B.150 C.7 1.1551 B.151 C.7 1.1552 B.152 C.71.1553 B.153 C.7 1.1554 B.154 C.7 1.1555 B.155 C.7 1.1556 B.156 C.71.1557 B.157 C.7 1.1558 B.158 C.7 1.1559 B.159 C.7 1.1560 B.160 C.71.1561 B.161 C.7 1.1562 B.162 C.7 1.1563 B.163 C.7 1.1564 B.164 C.71.1565 B.165 C.7 1.1566 B.166 C.7 1.1567 B.167 C.7 1.1568 B.168 C.71.1569 B.169 C.7 1.1570 B.170 C.7 1.1571 B.171 C.7 1.1572 B.172 C.71.1573 B.173 C.7 1.1574 B.174 C.7 1.1575 B.175 C.7 1.1576 B.176 C.71.1577 B.177 C.7 1.1578 B.178 C.7 1.1579 B.179 C.7 1.1580 B.180 C.71.1581 B.181 C.7 1.1582 B.182 C.7 1.1583 B.183 C.7 1.1584 B.184 C.71.1585 B.185 C.7 1.1586 B.186 C.7 1.1587 B.187 C.7 1.1588 B.188 C.71.1589 B.189 C.7 1.1590 B.190 C.7 1.1591 B.191 C.7 1.1592 B.192 C.71.1593 B.193 C.7 1.1594 B-194 C.7 1.1595 B-195 C.7 1.1596 B-196 C.71.1597 B-197 C.7 1.1598 B-198 C.7 1.1599 B-199 C.7 1.1600 B-200 C.71.1601 B.1 C.8 1.1602 B.2 C.8 1.1603 B.3 C.8 1.1604 B.4 C.8 1.1605 B.5C.8 1.1606 B.6 C.8 1.1607 B.7 C.8 1.1608 B.8 C.8 1.1609 B.9 C.8 1.1610B.10 C.8 1.1611 B.11 C.8 1.1612 B.12 C.8 1.1613 B.13 C.8 1.1614 B.14 C.81.1615 B.15 C.8 1.1616 B.16 C.8 1.1617 B.17 C.8 1.1618 B.18 C.8 1.1619B.19 C.8 1.1620 B.20 C.8 1.1621 B.21 C.8 1.1622 B.22 C.8 1.1623 B.23 C.81.1624 B.24 C.8 1.1625 B.25 C.8 1.1626 B.26 C.8 1.1627 B.27 C.8 1.1628B.28 C.8 1.1629 B.29 C.8 1.1630 B.30 C.8 1.1631 B.31 C.8 1.1632 B.32 C.81.1633 B.33 C.8 1.1634 B.34 C.8 1.1635 B.35 C.8 1.1636 B.36 C.8 1.1637B.37 C.8 1.1638 B.38 C.8 1.1639 B.39 C.8 1.1640 B.40 C.8 1.1641 B.41 C.81.1642 B.42 C.8 1.1643 B.43 C.8 1.1644 B.44 C.8 1.1645 B.45 C.8 1.1646B.46 C.8 1.1647 B.47 C.8 1.1648 B.48 C.8 1.1649 B.49 C.8 1.1650 B.50 C.81.1651 B.51 C.8 1.1652 B.52 C.8 1.1653 B.53 C.8 1.1654 B.54 C.8 1.1655B.55 C.8 1.1656 B.56 C.8 1.1657 B.57 C.8 1.1658 B.58. C.8 1.1659 B.59C.8 1.1660 B.60 C.8 1.1661 B.61 C.8 1.1662 B.62 C.8 1.1663 B.63 C.81.1664 B.64 C.8 1.1665 B.65 C.8 1.1666 B.66 C.8 1.1667 B.67 C.8 1.1668B.68 C.8 1.1669 B.69 C.8 1.1670 B.70 C.8 1.1671 B.71 C.8 1.1672 B.72 C.81.1673 B.73 C.8 1.1674 B.74 C.8 1.1675 B.75 C.8 1.1676 B.76 C.8 1.1677B.77 C.8 1.1678 B.78 C.8 1.1679 B.79 C.8 1.1680 B.80 C.8 1.1681 B.81 C.81.1682 B.82 C.8 1.1683 B.83 C.8 1.1684 B.84 C.8 1.1685 B.85 C.8 1.1686B.86 C.8 1.1687 B.87 C.8 1.1688 B.88 C.8 1.1689 B.89 C.8 1.1690 B.90 C.81.1691 B.91 C.8 1.1692 B.92 C.8 1.1693 B.93 C.8 1.1694 B.94 C.8 1.1695B.95 C.8 1.1696 B.96 C.8 1.1697 B.97 C.8 1.1698 B.98 C.8 1.1699 B.99 C.81.1700 B.100 C.8 1.1701 B.101 C.8 1.1702 B.102 C.8 1.1703 B.103 C.81.1704 B.104 C.8 1.1705 B.105 C.8 1.1706 B.106 C.8 1.1707 B.107 C.81.1708 B.108 C.8 1.1709 B.109 C.8 1.1710 B.110 C.8 1.1711 B.111 C.81.1712 B.112 C.8 1.1713 B.113 C.8 1.1714 B.114 C.8 1.1715 B.115 C.81.1716 B.116 C.8 1.1717 B.117 C.8 1.1718 B.118 C.8 1.1719 B.119 C.81.1720 B.120 C.8 1.1721 B.121 C.8 1.1722 B.122 C.8 1.1723 B.123 C.81.1724 B.124 C.8 1.1725 B.125 C.8 1.1726 B.126 C.8 1.1727 B.127 C.81.1728 B.128 C.8 1.1729 B.129 C.8 1.1730 B.130 C.8 1.1731 B.131 C.81.1732 B.132 C.8 1.1733 B.133 C.8 1.1734 B.134 C.8 1.1735 B.135 C.81.1736 B.136 C.8 1.1737 B.137 C.8 1.1738 B.138 C.8 1.1739 B.139 C.81.1740 B.140 C.8 1.1741 B.141 C.8 1.1742 B.142 C.8 1.1743 B.143 C.81.1744 B.144 C.8 1.1745 B.145 C.8 1.1746 B.146 C.8 1.1747 B.147 C.81.1748 B.148 C.8 1.1749 B.149 C.8 1.1750 B.150 C.8 1.1751 B.151 C.81.1752 B.152 C.8 1.1753 B.153 C.8 1.1754 B.154 C.8 1.1755 B.155 C.81.1756 B.156 C.8 1.1757 B.157 C.8 1.1758 B.158 C.8 1.1759 B.159 C.81.1760 B.160 C.8 1.1761 B.161 C.8 1.1762 B.162 C.8 1.1763 B.163 C.81.1764 B.164 C.8 1.1765 B.165 C.8 1.1766 B.166 C.8 1.1767 B.167 C.81.1768 B.168 C.8 1.1769 B.169 C.8 1.1770 B.170 C.8 1.1771 B.171 C.81.1772 B.172 C.8 1.1773 B.173 C.8 1.1774 B.174 C.8 1.1775 B.175 C.81.1776 B.176 C.8 1.1777 B.177 C.8 1.1778 B.178 C.8 1.1779 B.179 C.81.1780 B.180 C.8 1.1781 B.181 C.8 1.1782 B.182 C.8 1.1783 B.183 C.81.1784 B.184 C.8 1.1785 B.185 C.8 1.1786 B.186 C.8 1.1787 B.187 C.81.1788 B.188 C.8 1.1789 B.189 C.8 1.1790 B.190 C.8 1.1791 B.191 C.81.1792 B.192 C.8 1.1793 B.193 C.8 1.1794 B-194 C.8 1.1795 B-195 C.81.1796 B-196 C.8 1.1797 B-197 C.8 1.1798 B-198 C.8 1.1799 B-199 C.81.1800 B-200 C.8 1.1801 B.1 C.9 1.1802 B.2 C.9 1.1803 B.3 C.9 1.1804 B.4C.9 1.1805 B.5 C.9 1.1806 B.6 C.9 1.1807 B.7 C.9 1.1808 B.8 C.9 1.1809B.9 C.9 1.1810 B.10 C.9 1.1811 B.11 C.9 1.1812 B.12 C.9 1.1813 B.13 C.91.1814 B.14 C.9 1.1815 B.15 C.9 1.1816 B.16 C.9 1.1817 B.17 C.9 1.1818B.18 C.9 1.1819 B.19 C.9 1.1820 B.20 C.9 1.1821 B.21 C.9 1.1822 B.22 C.91.1823 B.23 C.9 1.1824 B.24 C.9 1.1825 B.25 C.9 1.1826 B.26 C.9 1.1827B.27 C.9 1.1828 B.28 C.9 1.1829 B.29 C.9 1.1830 B.30 C.9 1.1831 B.31 C.91.1832 B.32 C.9 1.1833 B.33 C.9 1.1834 B.34 C.9 1.1835 B.35 C.9 1.1836B.36 C.9 1.1837 B.37 C.9 1.1838 B.38 C.9 1.1839 B.39 C.9 1.1840 B.40 C.91.1841 B.41 C.9 1.1842 B.42 C.9 1.1843 B.43 C.9 1.1844 B.44 C.9 1.1845B.45 C.9 1.1846 B.46 C.9 1.1847 B.47 C.9 1.1848 B.48 C.9 1.1849 B.49 C.91.1850 B.50 C.9 1.1851 B.51 C.9 1.1852 B.52 C.9 1.1853 B.53 C.9 1.1854B.54 C.9 1.1855 B.55 C.9 1.1856 B.56 C.9 1.1857 B.57 C.9 1.1858 B.58.C.9 1.1859 B.59 C.9 1.1860 B.60 C.9 1.1861 B.61 C.9 1.1862 B.62 C.91.1863 B.63 C.9 1.1864 B.64 C.9 1.1865 B.65 C.9 1.1866 B.66 C.9 1.1867B.67 C.9 1.1868 B.68 C.9 1.1869 B.69 C.9 1.1870 B.70 C.9 1.1871 B.71 C.91.1872 B.72 C.9 1.1873 B.73 C.9 1.1874 B.74 C.9 1.1875 B.75 C.9 1.1876B.76 C.9 1.1877 B.77 C.9 1.1878 B.78 C.9 1.1879 B.79 C.9 1.1880 B.80 C.91.1881 B.81 C.9 1.1882 B.82 C.9 1.1883 B.83 C.9 1.1884 B.84 C.9 1.1885B.85 C.9 1.1886 B.86 C.9 1.1887 B.87 C.9 1.1888 B.88 C.9 1.1889 B.89 C.91.1890 B.90 C.9 1.1891 B.91 C.9 1.1892 B.92 C.9 1.1893 B.93 C.9 1.1894B.94 C.9 1.1895 B.95 C.9 1.1896 B.96 C.9 1.1897 B.97 C.9 1.1898 B.98 C.91.1899 B.99 C.9 1.1900 B.100 C.9 1.1901 B.101 C.9 1.1902 B.102 C.91.1903 B.103 C.9 1.1904 B.104 C.9 1.1905 B.105 C.9 1.1906 B.106 C.91.1907 B.107 C.9 1.1908 B.108 C.9 1.1909 B.109 C.9 1.1910 B.110 C.91.1911 B.111 C.9 1.1912 B.112 C.9 1.1913 B.113 C.9 1.1914 B.114 C.91.1915 B.115 C.9 1.1916 B.116 C.9 1.1917 B.117 C.9 1.1918 B.118 C.91.1919 B.119 C.9 1.1920 B.120 C.9 1.1921 B.121 C.9 1.1922 B.122 C.91.1923 B.123 C.9 1.1924 B.124 C.9 1.1925 B.125 C.9 1.1926 B.126 C.91.1927 B.127 C.9 1.1928 B.128 C.9 1.1929 B.129 C.9 1.1930 B.130 C.91.1931 B.131 C.9 1.1932 B.132 C.9 1.1933 B.133 C.9 1.1934 B.134 C.91.1935 B.135 C.9 1.1936 B.136 C.9 1.1937 B.137 C.9 1.1938 B.138 C.91.1939 B.139 C.9 1.1940 B.140 C.9 1.1941 B.141 C.9 1.1942 B.142 C.91.1943 B.143 C.9 1.1944 B.144 C.9 1.1945 B.145 C.9 1.1946 B.146 C.91.1947 B.147 C.9 1.1948 B.148 C.9 1.1949 B.149 C.9 1.1950 B.150 C.91.1951 B.151 C.9 1.1952 B.152 C.9 1.1953 B.153 C.9 1.1954 B.154 C.91.1955 B.155 C.9 1.1956 B.156 C.9 1.1957 B.157 C.9 1.1958 B.158 C.91.1959 B.159 C.9 1.1960 B.160 C.9 1.1961 B.161 C.9 1.1962 B.162 C.91.1963 B.163 C.9 1.1964 B.164 C.9 1.1965 B.165 C.9 1.1966 B.166 C.91.1967 B.167 C.9 1.1968 B.168 C.9 1.1969 B.169 C.9 1.1970 B.170 C.91.1971 B.171 C.9 1.1972 B.172 C.9 1.1973 B.173 C.9 1.1974 B.174 C.91.1975 B.175 C.9 1.1976 B.176 C.9 1.1977 B.177 C.9 1.1978 B.178 C.91.1979 B.179 C.9 1.1980 B.180 C.9 1.1981 B.181 C.9 1.1982 B.182 C.91.1983 B.183 C.9 1.1984 B.184 C.9 1.1985 B.185 C.9 1.1986 B.186 C.91.1987 B.187 C.9 1.1988 B.188 C.9 1.1989 B.189 C.9 1.1990 B.190 C.91.1991 B.191 C.9 1.1992 B.192 C.9 1.1993 B.193 C.9 1.1994 B-194 C.91.1995 B-195 C.9 1.1996 B-196 C.9 1.1997 B-197 C.9 1.1998 B-198 C.91.1999 B-199 C.9 1.2000 B-200 C.9 1.2001 B.1 C.10 1.2002 B.2 C.10 1.2003B.3 C.10 1.2004 B.4 C.10 1.2005 B.5 C.10 1.2006 B.6 C.10 1.2007 B.7 C.101.2008 B.8 C.10 1.2009 B.9 C.10 1.2010 B.10 C.10 1.2011 B.11 C.10 1.2012B.12 C.10 1.2013 B.13 C.10 1.2014 B.14 C.10 1.2015 B.15 C.10 1.2016 B.16C.10 1.2017 B.17 C.10 1.2018 B.18 C.10 1.2019 B.19 C.10 1.2020 B.20 C.101.2021 B.21 C.10 1.2022 B.22 C.10 1.2023 B.23 C.10 1.2024 B.24 C.101.2025 B.25 C.10 1.2026 B.26 C.10 1.2027 B.27 C.10 1.2028 B.28 C.101.2029 B.29 C.10 1.2030 B.30 C.10 1.2031 B.31 C.10 1.2032 B.32 C.101.2033 B.33 C.10 1.2034 B.34 C.10 1.2035 B.35 C.10 1.2036 B.36 C.101.2037 B.37 C.10 1.2038 B.38 C.10 1.2039 B.39 C.10 1.2040 B.40 C.101.2041 B.41 C.10 1.2042 B.42 C.10 1.2043 B.43 C.10 1.2044 B.44 C.101.2045 B.45 C.10 1.2046 B.46 C.10 1.2047 B.47 C.10 1.2048 B.48 C.101.2049 B.49 C.10 1.2050 B.50 C.10 1.2051 B.51 C.10 1.2052 B.52 C.101.2053 B.53 C.10 1.2054 B.54 C.10 1.2055 B.55 C.10 1.2056 B.56 C.101.2057 B.57 C.10 1.2058 B.58. C.10 1.2059 B.59 C.10 1.2060 B.60 C.101.2061 B.61 C.10 1.2062 B.62 C.10 1.2063 B.63 C.10 1.2064 B.64 C.101.2065 B.65 C.10 1.2066 B.66 C.10 1.2067 B.67 C.10 1.2068 B.68 C.101.2069 B.69 C.10 1.2070 B.70 C.10 1.2071 B.71 C.10 1.2072 B.72 C.101.2073 B.73 C.10 1.2074 B.74 C.10 1.2075 B.75 C.10 1.2076 B.76 C.101.2077 B.77 C.10 1.2078 B.78 C.10 1.2079 B.79 C.10 1.2080 B.80 C.101.2081 B.81 C.10 1.2082 B.82 C.10 1.2083 B.83 C.10 1.2084 B.84 C.101.2085 B.85 C.10 1.2086 B.86 C.10 1.2087 B.87 C.10 1.2088 B.88 C.101.2089 B.89 C.10 1.2090 B.90 C.10 1.2091 B.91 C.10 1.2092 B.92 C.101.2093 B.93 C.10 1.2094 B.94 C.10 1.2095 B.95 C.10 1.2096 B.96 C.101.2097 B.97 C.10 1.2098 B.98 C.10 1.2099 B.99 C.10 1.2100 B.100 C.101.2101 B.101 C.10 1.2102 B.102 C.10 1.2103 B.103 C.10 1.2104 B.104 C.101.2105 B.105 C.10 1.2106 B.106 C.10 1.2107 B.107 C.10 1.2108 B.108 C.101.2109 B.109 C.10 1.2110 B.110 C.10 1.2111 B.111 C.10 1.2112 B.112 C.101.2113 B.113 C.10 1.2114 B.114 C.10 1.2115 B.115 C.10 1.2116 B.116 C.101.2117 B.117 C.10 1.2118 B.118 C.10 1.2119 B.119 C.10 1.2120 B.120 C.101.2121 B.121 C.10 1.2122 B.122 C.10 1.2123 B.123 C.10 1.2124 B.124 C.101.2125 B.125 C.10 1.2126 B.126 C.10 1.2127 B.127 C.10 1.2128 B.128 C.101.2129 B.129 C.10 1.2130 B.130 C.10 1.2131 B.131 C.10 1.2132 B.132 C.101.2133 B.133 C.10 1.2134 B.134 C.10 1.2135 B.135 C.10 1.2136 B.136 C.101.2137 B.137 C.10 1.2138 B.138 C.10 1.2139 B.139 C.10 1.2140 B.140 C.101.2141 B.141 C.10 1.2142 B.142 C.10 1.2143 B.143 C.10 1.2144 B.144 C.101.2145 B.145 C.10 1.2146 B.146 C.10 1.2147 B.147 C.10 1.2148 B.148 C.101.2149 B.149 C.10 1.2150 B.150 C.10 1.2151 B.151 C.10 1.2152 B.152 C.101.2153 B.153 C.10 1.2154 B.154 C.10 1.2155 B.155 C.10 1.2156 B.156 C.101.2157 B.157 C.10 1.2158 B.158 C.10 1.2159 B.159 C.10 1.2160 B.160 C.101.2161 B.161 C.10 1.2162 B.162 C.10 1.2163 B.163 C.10 1.2164 B.164 C.101.2165 B.165 C.10 1.2166 B.166 C.10 1.2167 B.167 C.10 1.2168 B.168 C.101.2169 B.169 C.10 1.2170 B.170 C.10 1.2171 B.171 C.10 1.2172 B.172 C.101.2173 B.173 C.10 1.2174 B.174 C.10 1.2175 B.175 C.10 1.2176 B.176 C.101.2177 B.177 C.10 1.2178 B.178 C.10 1.2179 B.179 C.10 1.2180 B.180 C.101.2181 B.181 C.10 1.2182 B.182 C.10 1.2183 B.183 C.10 1.2184 B.184 C.101.2185 B.185 C.10 1.2186 B.186 C.10 1.2187 B.187 C.10 1.2188 B.188 C.101.2189 B.189 C.10 1.2190 B.190 C.10 1.2191 B.191 C.10 1.2192 B.192 C.101.2193 B.193 C.10 1.2194 B-194 C.10 1.2195 B-195 C.10 1.2196 B-196 C.101.2197 B-197 C.10 1.2198 B-198 C.10 1.2199 B-199 C.10 1.2200 B-200 C.101.2201 B.1 C.11 1.2202 B.2 C.11 1.2203 B.3 C.11 1.2204 B.4 C.11 1.2205B.5 C.11 1.2206 B.6 C.11 1.2207 B.7 C.11 1.2208 B.8 C.11 1.2209 B.9 C.111.2210 B.10 C.11 1.2211 B.11 C.11 1.2212 B.12 C.11 1.2213 B.13 C.111.2214 B.14 C.11 1.2215 B.15 C.11 1.2216 B.16 C.11 1.2217 B.17 C.111.2218 B.18 C.11 1.2219 B.19 C.11 1.2220 B.20 C.11 1.2221 B.21 C.111.2222 B.22 C.11 1.2223 B.23 C.11 1.2224 B.24 C.11 1.2225 B.25 C.111.2226 B.26 C.11 1.2227 B.27 C.11 1.2228 B.28 C.11 1.2229 B.29 C.111.2230 B.30 C.11 1.2231 B.31 C.11 1.2232 B.32 C.11 1.2233 B.33 C.111.2234 B.34 C.11 1.2235 B.35 C.11 1.2236 B.36 C.11 1.2237 B.37 C.111.2238 B.38 C.11 1.2239 B.39 C.11 1.2240 B.40 C.11 1.2241 B.41 C.111.2242 B.42 C.11 1.2243 B.43 C.11 1.2244 B.44 C.11 1.2245 B.45 C.111.2246 B.46 C.11 1.2247 B.47 C.11 1.2248 B.48 C.11 1.2249 B.49 C.111.2250 B.50 C.11 1.2251 B.51 C.11 1.2252 B.52 C.11 1.2253 B.53 C.111.2254 B.54 C.11 1.2255 B.55 C.11 1.2256 B.56 C.11 1.2257 B.57 C.111.2258 B.58. C.11 1.2259 B.59 C.11 1.2260 B.60 C.11 1.2261 B.61 C.111.2262 B.62 C.11 1.2263 B.63 C.11 1.2264 B.64 C.11 1.2265 B.65 C.111.2266 B.66 C.11 1.2267 B.67 C.11 1.2268 B.68 C.11 1.2269 B.69 C.111.2270 B.70 C.11 1.2271 B.71 C.11 1.2272 B.72 C.11 1.2273 B.73 C.111.2274 B.74 C.11 1.2275 B.75 C.11 1.2276 B.76 C.11 1.2277 B.77 C.111.2278 B.78 C.11 1.2279 B.79 C.11 1.2280 B.80 C.11 1.2281 B.81 C.111.2282 B.82 C.11 1.2283 B.83 C.11 1.2284 B.84 C.11 1.2285 B.85 C.111.2286 B.86 C.11 1.2287 B.87 C.11 1.2288 B.88 C.11 1.2289 B.89 C.111.2290 B.90 C.11 1.2291 B.91 C.11 1.2292 B.92 C.11 1.2293 B.93 C.111.2294 B.94 C.11 1.2295 B.95 C.11 1.2296 B.96 C.11 1.2297 B.97 C.111.2298 B.98 C.11 1.2299 B.99 C.11 1.2300 B.100 C.11 1.2301 B.101 C.111.2302 B.102 C.11 1.2303 B.103 C.11 1.2304 B.104 C.11 1.2305 B.105 C.111.2306 B.106 C.11 1.2307 B.107 C.11 1.2308 B.108 C.11 1.2309 B.109 C.111.2310 B.110 C.11 1.2311 B.111 C.11 1.2312 B.112 C.11 1.2313 B.113 C.111.2314 B.114 C.11 1.2315 B.115 C.11 1.2316 B.116 C.11 1.2317 B.117 C.111.2318 B.118 C.11 1.2319 B.119 C.11 1.2320 B.120 C.11 1.2321 B.121 C.111.2322 B.122 C.11 1.2323 B.123 C.11 1.2324 B.124 C.11 1.2325 B.125 C.111.2326 B.126 C.11 1.2327 B.127 C.11 1.2328 B.128 C.11 1.2329 B.129 C.111.2330 B.130 C.11 1.2331 B.131 C.11 1.2332 B.132 C.11 1.2333 B.133 C.111.2334 B.134 C.11 1.2335 B.135 C.11 1.2336 B.136 C.11 1.2337 B.137 C.111.2338 B.138 C.11 1.2339 B.139 C.11 1.2340 B.140 C.11 1.2341 B.141 C.111.2342 B.142 C.11 1.2343 B.143 C.11 1.2344 B.144 C.11 1.2345 B.145 C.111.2346 B.146 C.11 1.2347 B.147 C.11 1.2348 B.148 C.11 1.2349 B.149 C.111.2350 B.150 C.11 1.2351 B.151 C.11 1.2352 B.152 C.11 1.2353 B.153 C.111.2354 B.154 C.11 1.2355 B.155 C.11 1.2356 B.156 C.11 1.2357 B.157 C.111.2358 B.158 C.11 1.2359 B.159 C.11 1.2360 B.160 C.11 1.2361 B.161 C.111.2362 B.162 C.11 1.2363 B.163 C.11 1.2364 B.164 C.11 1.2365 B.165 C.111.2366 B.166 C.11 1.2367 B.167 C.11 1.2368 B.168 C.11 1.2369 B.169 C.111.2370 B.170 C.11 1.2371 B.171 C.11 1.2372 B.172 C.11 1.2373 B.173 C.111.2374 B.174 C.11 1.2375 B.175 C.11 1.2376 B.176 C.11 1.2377 B.177 C.111.2378 B.178 C.11 1.2379 B.179 C.11 1.2380 B.180 C.11 1.2381 B.181 C.111.2382 B.182 C.11 1.2383 B.183 C.11 1.2384 B.184 C.11 1.2385 B.185 C.111.2386 B.186 C.11 1.2387 B.187 C.11 1.2388 B.188 C.11 1.2389 B.189 C.111.2390 B.190 C.11 1.2391 B.191 C.11 1.2392 B.192 C.11 1.2393 B.193 C.111.2394 B-194 C.11 1.2395 B-195 C.11 1.2396 B-196 C.11 1.2397 B-197 C.111.2398 B-198 C.11 1.2399 B-199 C.11 1.2400 B-200 C.11 1.2401 B.1 C.121.2402 B.2 C.12 1.2403 B.3 C.12 1.2404 B.4 C.12 1.2405 B.5 C.12 1.2406B.6 C.12 1.2407 B.7 C.12 1.2408 B.8 C.12 1.2409 B.9 C.12 1.2410 B.10C.12 1.2411 B.11 C.12 1.2412 B.12 C.12 1.2413 B.13 C.12 1.2414 B.14 C.121.2415 B.15 C.12 1.2416 B.16 C.12 1.2417 B.17 C.12 1.2418 B.18 C.121.2419 B.19 C.12 1.2420 B.20 C.12 1.2421 B.21 C.12 1.2422 B.22 C.121.2423 B.23 C.12 1.2424 B.24 C.12 1.2425 B.25 C.12 1.2426 B.26 C.121.2427 B.27 C.12 1.2428 B.28 C.12 1.2429 B.29 C.12 1.2430 B.30 C.121.2431 B.31 C.12 1.2432 B.32 C.12 1.2433 B.33 C.12 1.2434 B.34 C.121.2435 B.35 C.12 1.2436 B.36 C.12 1.2437 B.37 C.12 1.2438 B.38 C.121.2439 B.39 C.12 1.2440 B.40 C.12 1.2441 B.41 C.12 1.2442 B.42 C.121.2443 B.43 C.12 1.2444 B.44 C.12 1.2445 B.45 C.12 1.2446 B.46 C.121.2447 B.47 C.12 1.2448 B.48 C.12 1.2449 B.49 C.12 1.2450 B.50 C.121.2451 B.51 C.12 1.2452 B.52 C.12 1.2453 B.53 C.12 1.2454 B.54 C.121.2455 B.55 C.12 1.2456 B.56 C.12 1.2457 B.57 C.12 1.2458 B.58. C.121.2459 B.59 C.12 1.2460 B.60 C.12 1.2461 B.61 C.12 1.2462 B.62 C.121.2463 B.63 C.12 1.2464 B.64 C.12 1.2465 B.65 C.12 1.2466 B.66 C.121.2467 B.67 C.12 1.2468 B.68 C.12 1.2469 B.69 C.12 1.2470 B.70 C.121.2471 B.71 C.12 1.2472 B.72 C.12 1.2473 B.73 C.12 1.2474 B.74 C.121.2475 B.75 C.12 1.2476 B.76 C.12 1.2477 B.77 C.12 1.2478 B.78 C.121.2479 B.79 C.12 1.2480 B.80 C.12 1.2481 B.81 C.12 1.2482 B.82 C.121.2483 B.83 C.12 1.2484 B.84 C.12 1.2485 B.85 C.12 1.2486 B.86 C.121.2487 B.87 C.12 1.2488 B.88 C.12 1.2489 B.89 C.12 1.2490 B.90 C.121.2491 B.91 C.12 1.2492 B.92 C.12 1.2493 B.93 C.12 1.2494 B.94 C.121.2495 B.95 C.12 1.2496 B.96 C.12 1.2497 B.97 C.12 1.2498 B.98 C.121.2499 B.99 C.12 1.2500 B.100 C.12 1.2501 B.101 C.12 1.2502 B.102 C.121.2503 B.103 C.12 1.2504 B.104 C.12 1.2505 B.105 C.12 1.2506 B.106 C.121.2507 B.107 C.12 1.2508 B.108 C.12 1.2509 B.109 C.12 1.2510 B.110 C.121.2511 B.111 C.12 1.2512 B.112 C.12 1.2513 B.113 C.12 1.2514 B.114 C.121.2515 B.115 C.12 1.2516 B.116 C.12 1.2517 B.117 C.12 1.2518 B.118 C.121.2519 B.119 C.12 1.2520 B.120 C.12 1.2521 B.121 C.12 1.2522 B.122 C.121.2523 B.123 C.12 1.2524 B.124 C.12 1.2525 B.125 C.12 1.2526 B.126 C.121.2527 B.127 C.12 1.2528 B.128 C.12 1.2529 B.129 C.12 1.2530 B.130 C.121.2531 B.131 C.12 1.2532 B.132 C.12 1.2533 B.133 C.12 1.2534 B.134 C.121.2535 B.135 C.12 1.2536 B.136 C.12 1.2537 B.137 C.12 1.2538 B.138 C.121.2539 B.139 C.12 1.2540 B.140 C.12 1.2541 B.141 C.12 1.2542 B.142 C.121.2543 B.143 C.12 1.2544 B.144 C.12 1.2545 B.145 C.12 1.2546 B.146 C.121.2547 B.147 C.12 1.2548 B.148 C.12 1.2549 B.149 C.12 1.2550 B.150 C.121.2551 B.151 C.12 1.2552 B.152 C.12 1.2553 B.153 C.12 1.2554 B.154 C.121.2555 B.155 C.12 1.2556 B.156 C.12 1.2557 B.157 C.12 1.2558 B.158 C.121.2559 B.159 C.12 1.2560 B.160 C.12 1.2561 B.161 C.12 1.2562 B.162 C.121.2563 B.163 C.12 1.2564 B.164 C.12 1.2565 B.165 C.12 1.2566 B.166 C.121.2567 B.167 C.12 1.2568 B.168 C.12 1.2569 B.169 C.12 1.2570 B.170 C.121.2571 B.171 C.12 1.2572 B.172 C.12 1.2573 B.173 C.12 1.2574 B.174 C.121.2575 B.175 C.12 1.2576 B.176 C.12 1.2577 B.177 C.12 1.2578 B.178 C.121.2579 B.179 C.12 1.2580 B.180 C.12 1.2581 B.181 C.12 1.2582 B.182 C.121.2583 B.183 C.12 1.2584 B.184 C.12 1.2585 B.185 C.12 1.2586 B.186 C.121.2587 B.187 C.12 1.2588 B.188 C.12 1.2589 B.189 C.12 1.2590 B.190 C.121.2591 B.191 C.12 1.2592 B.192 C.12 1.2593 B.193 C.12 1.2594 B-194 C.121.2595 B-195 C.12 1.2596 B-196 C.12 1.2597 B-197 C.12 1.2598 B-198 C.121.2599 B-199 C.12 1.2600 B-200 C.12 1.2601 B.1 C.13 1.2602 B.2 C.131.2603 B.3 C.13 1.2604 B.4 C.13 1.2605 B.5 C.13 1.2606 B.6 C.13 1.2607B.7 C.13 1.2608 B.8 C.13 1.2609 B.9 C.13 1.2610 B.10 C.13 1.2611 B.11C.13 1.2612 B.12 C.13 1.2613 B.13 C.13 1.2614 B.14 C.13 1.2615 B.15 C.131.2616 B.16 C.13 1.2617 B.17 C.13 1.2618 B.18 C.13 1.2619 B.19 C.131.2620 B.20 C.13 1.2621 B.21 C.13 1.2622 B.22 C.13 1.2623 B.23 C.131.2624 B.24 C.13 1.2625 B.25 C.13 1.2626 B.26 C.13 1.2627 B.27 C.131.2628 B.28 C.13 1.2629 B.29 C.13 1.2630 B.30 C.13 1.2631 B.31 C.131.2632 B.32 C.13 1.2633 B.33 C.13 1.2634 B.34 C.13 1.2635 B.35 C.131.2636 B.36 C.13 1.2637 B.37 C.13 1.2638 B.38 C.13 1.2639 B.39 C.131.2640 B.40 C.13 1.2641 B.41 C.13 1.2642 B.42 C.13 1.2643 B.43 C.131.2644 B.44 C.13 1.2645 B.45 C.13 1.2646 B.46 C.13 1.2647 B.47 C.131.2648 B.48 C.13 1.2649 B.49 C.13 1.2650 B.50 C.13 1.2651 B.51 C.131.2652 B.52 C.13 1.2653 B.53 C.13 1.2654 B.54 C.13 1.2655 B.55 C.131.2656 B.56 C.13 1.2657 B.57 C.13 1.2658 B.58. C.13 1.2659 B.59 C.131.2660 B.60 C.13 1.2661 B.61 C.13 1.2662 B.62 C.13 1.2663 B.63 C.131.2664 B.64 C.13 1.2665 B.65 C.13 1.2666 B.66 C.13 1.2667 B.67 C.131.2668 B.68 C.13 1.2669 B.69 C.13 1.2670 B.70 C.13 1.2671 B.71 C.131.2672 B.72 C.13 1.2673 B.73 C.13 1.2674 B.74 C.13 1.2675 B.75 C.131.2676 B.76 C.13 1.2677 B.77 C.13 1.2678 B.78 C.13 1.2679 B.79 C.131.2680 B.80 C.13 1.2681 B.81 C.13 1.2682 B.82 C.13 1.2683 B.83 C.131.2684 B.84 C.13 1.2685 B.85 C.13 1.2686 B.86 C.13 1.2687 B.87 C.131.2688 B.88 C.13 1.2689 B.89 C.13 1.2690 B.90 C.13 1.2691 B.91 C.131.2692 B.92 C.13 1.2693 B.93 C.13 1.2694 B.94 C.13 1.2695 B.95 C.131.2696 B.96 C.13 1.2697 B.97 C.13 1.2698 B.98 C.13 1.2699 B.99 C.131.2700 B.100 C.13 1.2701 B.101 C.13 1.2702 B.102 C.13 1.2703 B.103 C.131.2704 B.104 C.13 1.2705 B.105 C.13 1.2706 B.106 C.13 1.2707 B.107 C.131.2708 B.108 C.13 1.2709 B.109 C.13 1.2710 B.110 C.13 1.2711 B.111 C.131.2712 B.112 C.13 1.2713 B.113 C.13 1.2714 B.114 C.13 1.2715 B.115 C.131.2716 B.116 C.13 1.2717 B.117 C.13 1.2718 B.118 C.13 1.2719 B.119 C.131.2720 B.120 C.13 1.2721 B.121 C.13 1.2722 B.122 C.13 1.2723 B.123 C.131.2724 B.124 C.13 1.2725 B.125 C.13 1.2726 B.126 C.13 1.2727 B.127 C.131.2728 B.128 C.13 1.2729 B.129 C.13 1.2730 B.130 C.13 1.2731 B.131 C.131.2732 B.132 C.13 1.2733 B.133 C.13 1.2734 B.134 C.13 1.2735 B.135 C.131.2736 B.136 C.13 1.2737 B.137 C.13 1.2738 B.138 C.13 1.2739 B.139 C.131.2740 B.140 C.13 1.2741 B.141 C.13 1.2742 B.142 C.13 1.2743 B.143 C.131.2744 B.144 C.13 1.2745 B.145 C.13 1.2746 B.146 C.13 1.2747 B.147 C.131.2748 B.148 C.13 1.2749 B.149 C.13 1.2750 B.150 C.13 1.2751 B.151 C.131.2752 B.152 C.13 1.2753 B.153 C.13 1.2754 B.154 C.13 1.2755 B.155 C.131.2756 B.156 C.13 1.2757 B.157 C.13 1.2758 B.158 C.13 1.2759 B.159 C.131.2760 B.160 C.13 1.2761 B.161 C.13 1.2762 B.162 C.13 1.2763 B.163 C.131.2764 B.164 C.13 1.2765 B.165 C.13 1.2766 B.166 C.13 1.2767 B.167 C.131.2768 B.168 C.13 1.2769 B.169 C.13 1.2770 B.170 C.13 1.2771 B.171 C.131.2772 B.172 C.13 1.2773 B.173 C.13 1.2774 B.174 C.13 1.2775 B.175 C.131.2776 B.176 C.13 1.2777 B.177 C.13 1.2778 B.178 C.13 1.2779 B.179 C.131.2780 B.180 C.13 1.2781 B.181 C.13 1.2782 B.182 C.13 1.2783 B.183 C.131.2784 B.184 C.13 1.2785 B.185 C.13 1.2786 B.186 C.13 1.2787 B.187 C.131.2788 B.188 C.13 1.2789 B.189 C.13 1.2790 B.190 C.13 1.2791 B.191 C.131.2792 B.192 C.13 1.2793 B.193 C.13 1.2794 B-194 C.13 1.2795 B-195 C.131.2796 B-196 C.13 1.2797 B-197 C.13 1.2798 B-198 C.13 1.2799 B-199 C.131.2800 B-200 C.13 1.2801 B.1 C.14 1.2802 B.2 C.14 1.2803 B.3 C.14 1.2804B.4 C.14 1.2805 B.5 C.14 1.2806 B.6 C.14 1.2807 B.7 C.14 1.2808 B.8 C.141.2809 B.9 C.14 1.2810 B.10 C.14 1.2811 B.11 C.14 1.2812 B.12 C.141.2813 B.13 C.14 1.2814 B.14 C.14 1.2815 B.15 C.14 1.2816 B.16 C.141.2817 B.17 C.14 1.2818 B.18 C.14 1.2819 B.19 C.14 1.2820 B.20 C.141.2821 B.21 C.14 1.2822 B.22 C.14 1.2823 B.23 C.14 1.2824 B.24 C.141.2825 B.25 C.14 1.2826 B.26 C.14 1.2827 B.27 C.14 1.2828 B.28 C.141.2829 B.29 C.14 1.2830 B.30 C.14 1.2831 B.31 C.14 1.2832 B.32 C.141.2833 B.33 C.14 1.2834 B.34 C.14 1.2835 B.35 C.14 1.2836 B.36 C.141.2837 B.37 C.14 1.2838 B.38 C.14 1.2839 B.39 C.14 1.2840 B.40 C.141.2841 B.41 C.14 1.2842 B.42 C.14 1.2843 B.43 C.14 1.2844 B.44 C.141.2845 B.45 C.14 1.2846 B.46 C.14 1.2847 B.47 C.14 1.2848 B.48 C.141.2849 B.49 C.14 1.2850 B.50 C.14 1.2851 B.51 C.14 1.2852 B.52 C.141.2853 B.53 C.14 1.2854 B.54 C.14 1.2855 B.55 C.14 1.2856 B.56 C.141.2857 B.57 C.14 1.2858 B.58. C.14 1.2859 B.59 C.14 1.2860 B.60 C.141.2861 B.61 C.14 1.2862 B.62 C.14 1.2863 B.63 C.14 1.2864 B.64 C.141.2865 B.65 C.14 1.2866 B.66 C.14 1.2867 B.67 C.14 1.2868 B.68 C.141.2869 B.69 C.14 1.2870 B.70 C.14 1.2871 B.71 C.14 1.2872 B.72 C.141.2873 B.73 C.14 1.2874 B.74 C.14 1.2875 B.75 C.14 1.2876 B.76 C.141.2877 B.77 C.14 1.2878 B.78 C.14 1.2879 B.79 C.14 1.2880 B.80 C.141.2881 B.81 C.14 1.2882 B.82 C.14 1.2883 B.83 C.14 1.2884 B.84 C.141.2885 B.85 C.14 1.2886 B.86 C.14 1.2887 B.87 C.14 1.2888 B.88 C.141.2889 B.89 C.14 1.2890 B.90 C.14 1.2891 B.91 C.14 1.2892 B.92 C.141.2893 B.93 C.14 1.2894 B.94 C.14 1.2895 B.95 C.14 1.2896 B.96 C.141.2897 B.97 C.14 1.2898 B.98 C.14 1.2899 B.99 C.14 1.2900 B.100 C.141.2901 B.101 C.14 1.2902 B.102 C.14 1.2903 B.103 C.14 1.2904 B.104 C.141.2905 B.105 C.14 1.2906 B.106 C.14 1.2907 B.107 C.14 1.2908 B.108 C.141.2909 B.109 C.14 1.2910 B.110 C.14 1.2911 B.111 C.14 1.2912 B.112 C.141.2913 B.113 C.14 1.2914 B.114 C.14 1.2915 B.115 C.14 1.2916 B.116 C.141.2917 B.117 C.14 1.2918 B.118 C.14 1.2919 B.119 C.14 1.2920 B.120 C.141.2921 B.121 C.14 1.2922 B.122 C.14 1.2923 B.123 C.14 1.2924 B.124 C.141.2925 B.125 C.14 1.2926 B.126 C.14 1.2927 B.127 C.14 1.2928 B.128 C.141.2929 B.129 C.14 1.2930 B.130 C.14 1.2931 B.131 C.14 1.2932 B.132 C.141.2933 B.133 C.14 1.2934 B.134 C.14 1.2935 B.135 C.14 1.2936 B.136 C.141.2937 B.137 C.14 1.2938 B.138 C.14 1.2939 B.139 C.14 1.2940 B.140 C.141.2941 B.141 C.14 1.2942 B.142 C.14 1.2943 B.143 C.14 1.2944 B.144 C.141.2945 B.145 C.14 1.2946 B.146 C.14 1.2947 B.147 C.14 1.2948 B.148 C.141.2949 B.149 C.14 1.2950 B.150 C.14 1.2951 B.151 C.14 1.2952 B.152 C.141.2953 B.153 C.14 1.2954 B.154 C.14 1.2955 B.155 C.14 1.2956 B.156 C.141.2957 B.157 C.14 1.2958 B.158 C.14 1.2959 B.159 C.14 1.2960 B.160 C.141.2961 B.161 C.14 1.2962 B.162 C.14 1.2963 B.163 C.14 1.2964 B.164 C.141.2965 B.165 C.14 1.2966 B.166 C.14 1.2967 B.167 C.14 1.2968 B.168 C.141.2969 B.169 C.14 1.2970 B.170 C.14 1.2971 B.171 C.14 1.2972 B.172 C.141.2973 B.173 C.14 1.2974 B.174 C.14 1.2975 B.175 C.14 1.2976 B.176 C.141.2977 B.177 C.14 1.2978 B.178 C.14 1.2979 B.179 C.14 1.2980 B.180 C.141.2981 B.181 C.14 1.2982 B.182 C.14 1.2983 B.183 C.14 1.2984 B.184 C.141.2985 B.185 C.14 1.2986 B.186 C.14 1.2987 B.187 C.14 1.2988 B.188 C.141.2989 B.189 C.14 1.2990 B.190 C.14 1.2991 B.191 C.14 1.2992 B.192 C.141.2993 B.193 C.14 1.2994 B-194 C.14 1.2995 B-195 C.14 1.2996 B-196 C.141.2997 B-197 C.14 1.2998 B-198 C.14 1.2999 B-199 C.14 1.3000 B-200 C.141.3001 B.1 C.15 1.3002 B.2 C.15 1.3003 B.3 C.15 1.3004 B.4 C.15 1.3005B.5 C.15 1.3006 B.6 C.15 1.3007 B.7 C.15 1.3008 B.8 C.15 1.3009 B.9 C.151.3010 B.10 C.15 1.3011 B.11 C.15 1.3012 B.12 C.15 1.3013 B.13 C.151.3014 B.14 C.15 1.3015 B.15 C.15 1.3016 B.16 C.15 1.3017 B.17 C.151.3018 B.18 C.15 1.3019 B.19 C.15 1.3020 B.20 C.15 1.3021 B.21 C.151.3022 B.22 C.15 1.3023 B.23 C.15 1.3024 B.24 C.15 1.3025 B.25 C.151.3026 B.26 C.15 1.3027 B.27 C.15 1.3028 B.28 C.15 1.3029 B.29 C.151.3030 B.30 C.15 1.3031 B.31 C.15 1.3032 B.32 C.15 1.3033 B.33 C.151.3034 B.34 C.15 1.3035 B.35 C.15 1.3036 B.36 C.15 1.3037 B.37 C.151.3038 B.38 C.15 1.3039 B.39 C.15 1.3040 B.40 C.15 1.3041 B.41 C.151.3042 B.42 C.15 1.3043 B.43 C.15 1.3044 B.44 C.15 1.3045 B.45 C.151.3046 B.46 C.15 1.3047 B.47 C.15 1.3048 B.48 C.15 1.3049 B.49 C.151.3050 B.50 C.15 1.3051 B.51 C.15 1.3052 B.52 C.15 1.3053 B.53 C.151.3054 B.54 C.15 1.3055 B.55 C.15 1.3056 B.56 C.15 1.3057 B.57 C.151.3058 B.58. C.15 1.3059 B.59 C.15 1.3060 B.60 C.15 1.3061 B.61 C.151.3062 B.62 C.15 1.3063 B.63 C.15 1.3064 B.64 C.15 1.3065 B.65 C.151.3066 B.66 C.15 1.3067 B.67 C.15 1.3068 B.68 C.15 1.3069 B.69 C.151.3070 B.70 C.15 1.3071 B.71 C.15 1.3072 B.72 C.15 1.3073 B.73 C.151.3074 B.74 C.15 1.3075 B.75 C.15 1.3076 B.76 C.15 1.3077 B.77 C.151.3078 B.78 C.15 1.3079 B.79 C.15 1.3080 B.80 C.15 1.3081 B.81 C.151.3082 B.82 C.15 1.3083 B.83 C.15 1.3084 B.84 C.15 1.3085 B.85 C.151.3086 B.86 C.15 1.3087 B.87 C.15 1.3088 B.88 C.15 1.3089 B.89 C.151.3090 B.90 C.15 1.3091 B.91 C.15 1.3092 B.92 C.15 1.3093 B.93 C.151.3094 B.94 C.15 1.3095 B.95 C.15 1.3096 B.96 C.15 1.3097 B.97 C.151.3098 B.98 C.15 1.3099 B.99 C.15 1.3100 B.100 C.15 1.3101 B.101 C.151.3102 B.102 C.15 1.3103 B.103 C.15 1.3104 B.104 C.15 1.3105 B.105 C.151.3106 B.106 C.15 1.3107 B.107 C.15 1.3108 B.108 C.15 1.3109 B.109 C.151.3110 B.110 C.15 1.3111 B.111 C.15 1.3112 B.112 C.15 1.3113 B.113 C.151.3114 B.114 C.15 1.3115 B.115 C.15 1.3116 B.116 C.15 1.3117 B.117 C.151.3118 B.118 C.15 1.3119 B.119 C.15 1.3120 B.120 C.15 1.3121 B.121 C.151.3122 B.122 C.15 1.3123 B.123 C.15 1.3124 B.124 C.15 1.3125 B.125 C.151.3126 B.126 C.15 1.3127 B.127 C.15 1.3128 B.128 C.15 1.3129 B.129 C.151.3130 B.130 C.15 1.3131 B.131 C.15 1.3132 B.132 C.15 1.3133 B.133 C.151.3134 B.134 C.15 1.3135 B.135 C.15 1.3136 B.136 C.15 1.3137 B.137 C.151.3138 B.138 C.15 1.3139 B.139 C.15 1.3140 B.140 C.15 1.3141 B.141 C.151.3142 B.142 C.15 1.3143 B.143 C.15 1.3144 B.144 C.15 1.3145 B.145 C.151.3146 B.146 C.15 1.3147 B.147 C.15 1.3148 B.148 C.15 1.3149 B.149 C.151.3150 B.150 C.15 1.3151 B.151 C.15 1.3152 B.152 C.15 1.3153 B.153 C.151.3154 B.154 C.15 1.3155 B.155 C.15 1.3156 B.156 C.15 1.3157 B.157 C.151.3158 B.158 C.15 1.3159 B.159 C.15 1.3160 B.160 C.15 1.3161 B.161 C.151.3162 B.162 C.15 1.3163 B.163 C.15 1.3164 B.164 C.15 1.3165 B.165 C.151.3166 B.166 C.15 1.3167 B.167 C.15 1.3168 B.168 C.15 1.3169 B.169 C.151.3170 B.170 C.15 1.3171 B.171 C.15 1.3172 B.172 C.15 1.3173 B.173 C.151.3174 B.174 C.15 1.3175 B.175 C.15 1.3176 B.176 C.15 1.3177 B.177 C.151.3178 B.178 C.15 1.3179 B.179 C.15 1.3180 B.180 C.15 1.3181 B.181 C.151.3182 B.182 C.15 1.3183 B.183 C.15 1.3184 B.184 C.15 1.3185 B.185 C.151.3186 B.186 C.15 1.3187 B.187 C.15 1.3188 B.188 C.15 1.3189 B.189 C.151.3190 B.190 C.15 1.3191 B.191 C.15 1.3192 B.192 C.15 1.3193 B.193 C.151.3194 B-194 C.15 1.3195 B-195 C.15 1.3196 B-196 C.15 1.3197 B-197 C.151.3198 B-198 C.15 1.3199 B-199 C.15 1.3200 B-200 C.15 1.3201 B.1 C.161.3202 B.2 C.16 1.3203 B.3 C.16 1.3204 B.4 C.16 1.3205 B.5 C.16 1.3206B.6 C.16 1.3207 B.7 C.16 1.3208 B.8 C.16 1.3209 B.9 C.16 1.3210 B.10C.16 1.3211 B.11 C.16 1.3212 B.12 C.16 1.3213 B.13 C.16 1.3214 B.14 C.161.3215 B.15 C.16 1.3216 B.16 C.16 1.3217 B.17 C.16 1.3218 B.18 C.161.3219 B.19 C.16 1.3220 B.20 C.16 1.3221 B.21 C.16 1.3222 B.22 C.161.3223 B.23 C.16 1.3224 B.24 C.16 1.3225 B.25 C.16 1.3226 B.26 C.161.3227 B.27 C.16 1.3228 B.28 C.16 1.3229 B.29 C.16 1.3230 B.30 C.161.3231 B.31 C.16 1.3232 B.32 C.16 1.3233 B.33 C.16 1.3234 B.34 C.161.3235 B.35 C.16 1.3236 B.36 C.16 1.3237 B.37 C.16 1.3238 B.38 C.161.3239 B.39 C.16 1.3240 B.40 C.16 1.3241 B.41 C.16 1.3242 B.42 C.161.3243 B.43 C.16 1.3244 B.44 C.16 1.3245 B.45 C.16 1.3246 B.46 C.161.3247 B.47 C.16 1.3248 B.48 C.16 1.3249 B.49 C.16 1.3250 B.50 C.161.3251 B.51 C.16 1.3252 B.52 C.16 1.3253 B.53 C.16 1.3254 B.54 C.161.3255 B.55 C.16 1.3256 B.56 C.16 1.3257 B.57 C.16 1.3258 B.58. C.161.3259 B.59 C.16 1.3260 B.60 C.16 1.3261 B.61 C.16 1.3262 B.62 C.161.3263 B.63 C.16 1.3264 B.64 C.16 1.3265 B.65 C.16 1.3266 B.66 C.161.3267 B.67 C.16 1.3268 B.68 C.16 1.3269 B.69 C.16 1.3270 B.70 C.161.3271 B.71 C.16 1.3272 B.72 C.16 1.3273 B.73 C.16 1.3274 B.74 C.161.3275 B.75 C.16 1.3276 B.76 C.16 1.3277 B.77 C.16 1.3278 B.78 C.161.3279 B.79 C.16 1.3280 B.80 C.16 1.3281 B.81 C.16 1.3282 B.82 C.161.3283 B.83 C.16 1.3284 B.84 C.16 1.3285 B.85 C.16 1.3286 B.86 C.161.3287 B.87 C.16 1.3288 B.88 C.16 1.3289 B.89 C.16 1.3290 B.90 C.161.3291 B.91 C.16 1.3292 B.92 C.16 1.3293 B.93 C.16 1.3294 B.94 C.161.3295 B.95 C.16 1.3296 B.96 C.16 1.3297 B.97 C.16 1.3298 B.98 C.161.3299 B.99 C.16 1.3300 B.100 C.16 1.3301 B.101 C.16 1.3302 B.102 C.161.3303 B.103 C.16 1.3304 B.104 C.16 1.3305 B.105 C.16 1.3306 B.106 C.161.3307 B.107 C.16 1.3308 B.108 C.16 1.3309 B.109 C.16 1.3310 B.110 C.161.3311 B.111 C.16 1.3312 B.112 C.16 1.3313 B.113 C.16 1.3314 B.114 C.161.3315 B.115 C.16 1.3316 B.116 C.16 1.3317 B.117 C.16 1.3318 B.118 C.161.3319 B.119 C.16 1.3320 B.120 C.16 1.3321 B.121 C.16 1.3322 B.122 C.161.3323 B.123 C.16 1.3324 B.124 C.16 1.3325 B.125 C.16 1.3326 B.126 C.161.3327 B.127 C.16 1.3328 B.128 C.16 1.3329 B.129 C.16 1.3330 B.130 C.161.3331 B.131 C.16 1.3332 B.132 C.16 1.3333 B.133 C.16 1.3334 B.134 C.161.3335 B.135 C.16 1.3336 B.136 C.16 1.3337 B.137 C.16 1.3338 B.138 C.161.3339 B.139 C.16 1.3340 B.140 C.16 1.3341 B.141 C.16 1.3342 B.142 C.161.3343 B.143 C.16 1.3344 B.144 C.16 1.3345 B.145 C.16 1.3346 B.146 C.161.3347 B.147 C.16 1.3348 B.148 C.16 1.3349 B.149 C.16 1.3350 B.150 C.161.3351 B.151 C.16 1.3352 B.152 C.16 1.3353 B.153 C.16 1.3354 B.154 C.161.3355 B.155 C.16 1.3356 B.156 C.16 1.3357 B.157 C.16 1.3358 B.158 C.161.3359 B.159 C.16 1.3360 B.160 C.16 1.3361 B.161 C.16 1.3362 B.162 C.161.3363 B.163 C.16 1.3364 B.164 C.16 1.3365 B.165 C.16 1.3366 B.166 C.161.3367 B.167 C.16 1.3368 B.168 C.16 1.3369 B.169 C.16 1.3370 B.170 C.161.3371 B.171 C.16 1.3372 B.172 C.16 1.3373 B.173 C.16 1.3374 B.174 C.161.3375 B.175 C.16 1.3376 B.176 C.16 1.3377 B.177 C.16 1.3378 B.178 C.161.3379 B.179 C.16 1.3380 B.180 C.16 1.3381 B.181 C.16 1.3382 B.182 C.161.3383 B.183 C.16 1.3384 B.184 C.16 1.3385 B.185 C.16 1.3386 B.186 C.161.3387 B.187 C.16 1.3388 B.188 C.16 1.3389 B.189 C.16 1.3390 B.190 C.161.3391 B.191 C.16 1.3392 B.192 C.16 1.3393 B.193 C.16 1.3394 B-194 C.161.3395 B-195 C.16 1.3396 B-196 C.16 1.3397 B-197 C.16 1.3398 B-198 C.161.3399 B-199 C.16 1.3400 B-200 C.16 1.3401 B.1 C.17 1.3402 B.2 C.171.3403 B.3 C.17 1.3404 B.4 C.17 1.3405 B.5 C.17 1.3406 B.6 C.17 1.3407B.7 C.17 1.3408 B.8 C.17 1.3409 B.9 C.17 1.3410 B.10 C.17 1.3411 B.11C.17 1.3412 B.12 C.17 1.3413 B.13 C.17 1.3414 B.14 C.17 1.3415 B.15 C.171.3416 B.16 C.17 1.3417 B.17 C.17 1.3418 B.18 C.17 1.3419 B.19 C.171.3420 B.20 C.17 1.3421 B.21 C.17 1.3422 B.22 C.17 1.3423 B.23 C.171.3424 B.24 C.17 1.3425 B.25 C.17 1.3426 B.26 C.17 1.3427 B.27 C.171.3428 B.28 C.17 1.3429 B.29 C.17 1.3430 B.30 C.17 1.3431 B.31 C.171.3432 B.32 C.17 1.3433 B.33 C.17 1.3434 B.34 C.17 1.3435 B.35 C.171.3436 B.36 C.17 1.3437 B.37 C.17 1.3438 B.38 C.17 1.3439 B.39 C.171.3440 B.40 C.17 1.3441 B.41 C.17 1.3442 B.42 C.17 1.3443 B.43 C.171.3444 B.44 C.17 1.3445 B.45 C.17 1.3446 B.46 C.17 1.3447 B.47 C.171.3448 B.48 C.17 1.3449 B.49 C.17 1.3450 B.50 C.17 1.3451 B.51 C.171.3452 B.52 C.17 1.3453 B.53 C.17 1.3454 B.54 C.17 1.3455 B.55 C.171.3456 B.56 C.17 1.3457 B.57 C.17 1.3458 B.58. C.17 1.3459 B.59 C.171.3460 B.60 C.17 1.3461 B.61 C.17 1.3462 B.62 C.17 1.3463 B.63 C.171.3464 B.64 C.17 1.3465 B.65 C.17 1.3466 B.66 C.17 1.3467 B.67 C.171.3468 B.68 C.17 1.3469 B.69 C.17 1.3470 B.70 C.17 1.3471 B.71 C.171.3472 B.72 C.17 1.3473 B.73 C.17 1.3474 B.74 C.17 1.3475 B.75 C.171.3476 B.76 C.17 1.3477 B.77 C.17 1.3478 B.78 C.17 1.3479 B.79 C.171.3480 B.80 C.17 1.3481 B.81 C.17 1.3482 B.82 C.17 1.3483 B.83 C.171.3484 B.84 C.17 1.3485 B.85 C.17 1.3486 B.86 C.17 1.3487 B.87 C.171.3488 B.88 C.17 1.3489 B.89 C.17 1.3490 B.90 C.17 1.3491 B.91 C.171.3492 B.92 C.17 1.3493 B.93 C.17 1.3494 B.94 C.17 1.3495 B.95 C.171.3496 B.96 C.17 1.3497 B.97 C.17 1.3498 B.98 C.17 1.3499 B.99 C.171.3500 B.100 C.17 1.3501 B.101 C.17 1.3502 B.102 C.17 1.3503 B.103 C.171.3504 B.104 C.17 1.3505 B.105 C.17 1.3506 B.106 C.17 1.3507 B.107 C.171.3508 B.108 C.17 1.3509 B.109 C.17 1.3510 B.110 C.17 1.3511 B.111 C.171.3512 B.112 C.17 1.3513 B.113 C.17 1.3514 B.114 C.17 1.3515 B.115 C.171.3516 B.116 C.17 1.3517 B.117 C.17 1.3518 B.118 C.17 1.3519 B.119 C.171.3520 B.120 C.17 1.3521 B.121 C.17 1.3522 B.122 C.17 1.3523 B.123 C.171.3524 B.124 C.17 1.3525 B.125 C.17 1.3526 B.126 C.17 1.3527 B.127 C.171.3528 B.128 C.17 1.3529 B.129 C.17 1.3530 B.130 C.17 1.3531 B.131 C.171.3532 B.132 C.17 1.3533 B.133 C.17 1.3534 B.134 C.17 1.3535 B.135 C.171.3536 B.136 C.17 1.3537 B.137 C.17 1.3538 B.138 C.17 1.3539 B.139 C.171.3540 B.140 C.17 1.3541 B.141 C.17 1.3542 B.142 C.17 1.3543 B.143 C.171.3544 B.144 C.17 1.3545 B.145 C.17 1.3546 B.146 C.17 1.3547 B.147 C.171.3548 B.148 C.17 1.3549 B.149 C.17 1.3550 B.150 C.17 1.3551 B.151 C.171.3552 B.152 C.17 1.3553 B.153 C.17 1.3554 B.154 C.17 1.3555 B.155 C.171.3556 B.156 C.17 1.3557 B.157 C.17 1.3558 B.158 C.17 1.3559 B.159 C.171.3560 B.160 C.17 1.3561 B.161 C.17 1.3562 B.162 C.17 1.3563 B.163 C.171.3564 B.164 C.17 1.3565 B.165 C.17 1.3566 B.166 C.17 1.3567 B.167 C.171.3568 B.168 C.17 1.3569 B.169 C.17 1.3570 B.170 C.17 1.3571 B.171 C.171.3572 B.172 C.17 1.3573 B.173 C.17 1.3574 B.174 C.17 1.3575 B.175 C.171.3576 B.176 C.17 1.3577 B.177 C.17 1.3578 B.178 C.17 1.3579 B.179 C.171.3580 B.180 C.17 1.3581 B.181 C.17 1.3582 B.182 C.17 1.3583 B.183 C.171.3584 B.184 C.17 1.3585 B.185 C.17 1.3586 B.186 C.17 1.3587 B.187 C.171.3588 B.188 C.17 1.3589 B.189 C.17 1.3590 B.190 C.17 1.3591 B.191 C.171.3592 B.192 C.17 1.3593 B.193 C.17 1.3594 B-194 C.17 1.3595 B-195 C.171.3596 B-196 C.17 1.3597 B-197 C.17 1.3598 B-198 C.17 1.3599 B-199 C.171.3600 B-200 C.17 1.3601 — C.1 1.3602 — C.2 1.3603 — C.3 1.3604 — C.41.3605 — C.5 1.3606 — C.6 1.3607 — C.7 1.3608 — C.8 1.3609 — C.9 1.3610— C.10 1.3611 — C.11 1.3612 — C.12 1.3613 — C.13 1.3614 — C.14 1.3615 —C.15 1.3616 — C.16 1.3617 — C.17

The specific number for each single composition is deductible asfollows:

Composition 1.854 for example comprises a compound of the formula (I.1),pyrazosulfuron-ethyl (B.54) and cyprosulfamide (C.4) (see table 1, entry1.854; as well as table B, entry B.54 and table C, entry C.4).

Also especially preferred are compositions 2.1 to 2.3617 which differfrom the corresponding compositions 1.1 to 1.3617 only in that theycomprise as the active component A, instead of theisoxazolo[5,4-b]pyridine of formula (I.1), the anisoxazolo[5,4-b]pyridine of formula (I.2).

Also especially preferred are compositions 3.1 to 3.3617 which differfrom the corresponding compositions 1.1 to 1.3617 only in that theycomprise as the active compound A, instead of the anisoxazolo[5,4-b]pyridine of formula (I.1), the anisoxazolo[5,4-b]pyridine of formula (I.3).

Also especially preferred are compositions 1a.1 to 1a.3617, 2a.1 to2a.3617, 3a.1 to 3a.3617 which differ from the correspondingcompositions 1.1 to 1.3617, 2.1 to 2.3617 and 3.1 to 3.3617,respectively, only in that they comprise as the component A anisoxazolo[5,4-b]pyridine of formula (I.1), (I.2) or (I.3), respectively,each in the form of its carboxylic acid ester, thioester or amide formedwith the carboxylic acid moiety of the isoxazolo[5,4-b]pyridine of theformula (I).

Also especially preferred are compositions 4.1 to 4.3617 which differfrom the corresponding compositions 1.1 to 1.3617 only in that theyadditionally comprise B.8 pinoxaden as further herbicide B.

Also especially preferred are compositions 5.1 to 5.3617 which differfrom the corresponding compositions 1.1 to 1.3617 only in that theyadditionally comprise B.30 imazamox as further herbicide B.

Also especially preferred are compositions 6.1 to 6.3617 which differfrom the corresponding compositions 1.1 to 1.3617 only in that theyadditionally comprise B.32 imazapic as further herbicide B.

Also especially preferred are compositions 7.1 to 7.3617 which differfrom the corresponding compositions 1.1 to 1.3617 only in that theyadditionally comprise B.35 imazapyr as further herbicide B.

Also especially preferred are compositions 8.1 to 8.3617 which differfrom the corresponding compositions 1.1 to 1.3617 only in that theyadditionally comprise B.38 imazaquin as further herbicide B.

Also especially preferred are compositions 9.1 to 9.3617 which differfrom the corresponding compositions 1.1 to 1.3617 only in that theyadditionally comprise B.40 imazethapyr as further herbicide B.

Also especially preferred are compositions 10.1 to 10.3617 which differfrom the corresponding compositions 1.1 to 1.3617 only in that theyadditionally comprise B.51 nicosulfuron as further herbicide B.

Also especially preferred are compositions 11.1 to 11.3617 which differfrom the corresponding compositions 1.1 to 1.3617 only in that theyadditionally comprise B.55 pyribenzoxim as further herbicide B.

Also especially preferred are compositions 12.1 to 12.3617 which differfrom the corresponding compositions 1.1 to 1.3617 only in that theyadditionally comprise B.56 pyriftalid as further herbicide B.

Also especially preferred are compositions 13.1 to 13.3617 which differfrom the corresponding compositions 1.1 to 1.3617 only in that theyadditionally comprise B.64 tritosulfuron as further herbicide B.

Also especially preferred are compositions 14.1 to 14.3617 which differfrom the corresponding compositions 1.1 to 1.3617 only in that theyadditionally comprise B.66 ametryne as further herbicide B.

Also especially preferred are compositions 15.1 to 15.3617 which differfrom the corresponding compositions 1.1 to 1.3617 only in that theyadditionally comprise B.67 atrazine as further herbicide B.

Also especially preferred are compositions 16.1 to 16.3617 which differfrom the corresponding compositions 1.1 to 1.3617 only in that theyadditionally comprise B.68 bentazon as further herbicide B.

Also especially preferred are compositions 17.1 to 17.3617 which differfrom the corresponding compositions 1.1 to 1.3617 only in that theyadditionally comprise B.69 bromoxynil as further herbicide B.

Also especially preferred are compositions 18.1 to 18.3617 which differfrom the corresponding compositions 1.1 to 1.3617 only in that theyadditionally comprise B.73 diuron as further herbicide B.

Also especially preferred are compositions 19.1 to 19.3617 which differfrom the corresponding compositions 1.1 to 1.3617 only in that theyadditionally comprise B.76 isoproturon as further herbicide B.

Also especially preferred are compositions 20.1 to 20.3617 which differfrom the corresponding compositions 1.1 to 1.3617 only in that theyadditionally comprise B.81 simazin as further herbicide B.

Also especially preferred are compositions 21.1 to 21.3617 which differfrom the corresponding compositions 1.1 to 1.3617 only in that theyadditionally comprise B.82 terbuthylazin as further herbicide B.

Also especially preferred are compositions 22.1 to 22.3617 which differfrom the corresponding compositions 1.1 to 1.3617 only in that theyadditionally comprise B.85 acifluorfen as further herbicide B.

Also especially preferred are compositions 23.1 to 23.3617 which differfrom the corresponding compositions 1.1 to 1.3617 only in that theyadditionally comprise B.88 flumioxazin as further herbicide B.

Also especially preferred are compositions 24.1 to 24.3617 which differfrom the corresponding compositions 1.1 to 1.3617 only in that theyadditionally comprise B.89 fomesafen as further herbicide B.

Also especially preferred are compositions 25.1 to 25.3617 which differfrom the corresponding compositions 1.1 to 1.3617 only in that theyadditionally comprise B.92 saflufenacil as further herbicide B.

Also especially preferred are compositions 26.1 to 26.3617 which differfrom the corresponding compositions 1.1 to 1.3617 only in that theyadditionally comprise B.93 sulfentrazone as further herbicide B.

Also especially preferred are compositions 27.1 to 27.3617 which differfrom the corresponding compositions 1.1 to 1.3617 only in that theyadditionally comprise B.96 benzbicyclone as further herbicide B.

Also especially preferred are compositions 28.1 to 28.3617 which differfrom the corresponding compositions 1.1 to 1.3617 only in that theyadditionally comprise B.97 clomazone as further herbicide B.

Also especially preferred are compositions 29.1 to 29.3617 which differfrom the corresponding compositions 1.1 to 1.3617 only in that theyadditionally comprise B.100 isoxaflutole as further herbicide B.

Also especially preferred are compositions 30.1 to 30.3617 which differfrom the corresponding compositions 1.1 to 1.3617 only in that theyadditionally comprise B.100 isoxaflutole and B.67 atrazine as furtherherbicides B.

Also especially preferred are compositions 31.1 to 31.3617 which differfrom the corresponding compositions 1.1 to 1.3617 only in that theyadditionally comprise B.100 isoxaflutole and B.76 isoproturon as furtherherbicides B.

Also especially preferred are compositions 32.1 to 32.3617 which differfrom the corresponding compositions 1.1 to 1.3617 only in that theyadditionally comprise B.100 isoxaflutole and B.82 terbutylazin asfurther herbicides B.

Also especially preferred are compositions 33.1 to 33.3617 which differfrom the corresponding compositions 1.1 to 1.3617 only in that theyadditionally comprise B.101 mesotrione as further herbicide B.

Also especially preferred are compositions 34.1 to 34.3617 which differfrom the corresponding compositions 1.1 to 1.3617 only in that theyadditionally comprise B.101 mesotrione and B.67 atrazine as furtherherbicides B.

Also especially preferred are compositions 35.1 to 35.3617 which differfrom the corresponding compositions 1.1 to 1.3617 only in that theyadditionally comprise B.101 mesotrione and B.76 isoproturon as furtherherbicides B.

Also especially preferred are compositions 36.1 to 36.3617 which differfrom the corresponding compositions 1.1 to 1.3617 only in that theyadditionally comprise B.101 mesotrione and B.82 terbutylazin as furtherherbicides B.

Also especially preferred are compositions 37.1 to 37.3617 which differfrom the corresponding compositions 1.1 to 1.3617 only in that theyadditionally comprise B.103 picolinafen as further herbicide B.

Also especially preferred are compositions 38.1 to 38.3617 which differfrom the corresponding compositions 1.1 to 1.3617 only in that theyadditionally comprise B.104 sulcotrione as further herbicide B.

Also especially preferred are compositions 39.1 to 39.3617 which differfrom the corresponding compositions 1.1 to 1.3617 only in that theyadditionally comprise B. 104 sulcotrione and B.67 atrazine as furtherherbicides B.

Also especially preferred are compositions 40.1 to 40.3617 which differfrom the corresponding compositions 1.1 to 1.3617 only in that theyadditionally comprise B. 104 sulcotrione and B.76 isoproturon as furtherherbicides B.

Also especially preferred are compositions 41.1 to 41.3617 which differfrom the corresponding compositions 1.1 to 1.3617 only in that theyadditionally comprise B. 104 sulcotrione and B.82 terbutylazin asfurther herbicides B.

Also especially preferred are compositions 42.1 to 42.3617 which differfrom the corresponding compositions 1.1 to 1.3617 only in that theyadditionally comprise B.106 tembotrione as further herbicide B.

Also especially preferred are compositions 43.1 to 43.3617 which differfrom the corresponding compositions 1.1 to 1.3617 only in that theyadditionally comprise B.107 topramezone as further herbicide B.

Also especially preferred are compositions 44.1 to 44.3617 which differfrom the corresponding compositions 1.1 to 1.3617 only in that theyadditionally comprise B.107 topramezone and B.67 atrazine as furtherherbicides B.

Also especially preferred are compositions 45.1 to 45.3617 which differfrom the corresponding compositions 1.1 to 1.3617 only in that theyadditionally comprise B.107 topramezone and B.76 isoproturon as furtherherbicides B.

Also especially preferred are compositions 46.1 to 46.3617 which differfrom the corresponding compositions 1.1 to 1.3617 only in that theyadditionally comprise B.107 topramezone and B.82 terbutylazin as furtherherbicides B.

Also especially preferred are compositions 47.1 to 47.3617 which differfrom the corresponding compositions 1.1 to 1.3617 only in that theyadditionally comprise B.112 glyphosate as further herbicide B.

Also especially preferred are compositions 48.1 to 48.3617 which differfrom the corresponding compositions 1.1 to 1.3617 only in that theyadditionally comprise B.112 glyphosate and B.67 atrazine as furtherherbicides B.

Also especially preferred are compositions 49.1 to 49.3617 which differfrom the corresponding compositions 1.1 to 1.3617 only in that theyadditionally comprise B.112 glyphosate and B.92 saflufenacil as furtherherbicides B.

Also especially preferred are compositions 50.1 to 50.3617 which differfrom the corresponding compositions 1.1 to 1.3617 only in that theyadditionally comprise B.112 glyphosate and B.100 isoxaflutole as furtherherbicides B.

Also especially preferred are compositions 51.1 to 51.3617 which differfrom the corresponding compositions 1.1 to 1.3617 only in that theyadditionally comprise B.112 glyphosate and B.124 acetochlor as furtherherbicides B.

Also especially preferred are compositions 52.1 to 52.3617 which differfrom the corresponding compositions 1.1 to 1.3617 only in that theyadditionally comprise B.112 glyphosate and B.101 mesotrione as furtherherbicides B.

Also especially preferred are compositions 53.1 to 53.3617 which differfrom the corresponding compositions 1.1 to 1.3617 only in that theyadditionally comprise B.112 glyphosate and B.104 sulcotrione as furtherherbicides B.

Also especially preferred are compositions 54.1 to 54.3617 which differfrom the corresponding compositions 1.1 to 1.3617 only in that theyadditionally comprise B.112 glyphosate and B.107 topramezone as furtherherbicides B.

Also especially preferred are compositions 55.1 to 55.3617 which differfrom the corresponding compositions 1.1 to 1.3617 only in that theyadditionally comprise B.118 glufosinate as further herbicide B.

Also especially preferred are compositions 56.1 to 56.3617 which differfrom the corresponding compositions 1.1 to 1.3617 only in that theyadditionally comprise B.122 pendimethalin as further herbicide B.

Also especially preferred are compositions 57.1 to 57.3617 which differfrom the corresponding compositions 1.1 to 1.3617 only in that theyadditionally comprise B.124 acetochlor as further herbicide B.

Also especially preferred are compositions 58.1 to 58.3617 which differfrom the corresponding compositions 1.1 to 1.3617 only in that theyadditionally comprise B.127 dimethenamid-P as further herbicide B.

Also especially preferred are compositions 59.1 to 59.3617 which differfrom the corresponding compositions 1.1 to 1.3617 only in that theyadditionally comprise B.128 fentrazamide as further herbicide B.

Also especially preferred are compositions 60.1 to 60.3617 which differfrom the corresponding compositions 1.1 to 1.3617 only in that theyadditionally comprise B.129 flufenacet as further herbicide B.

Also especially preferred are compositions 61.1 to 61.3617 which differfrom the corresponding compositions 1.1 to 1.3617 only in that theyadditionally comprise B.131 metazachlor as further herbicide B.

Also especially preferred are compositions 62.1 to 62.3617 which differfrom the corresponding compositions 1.1 to 1.3617 only in that theyadditionally comprise B.133 S-metolachlor as further herbicide B.

Also especially preferred are compositions 63.1 to 63.3617 which differfrom the corresponding compositions 11.1 to 1.3617 only in that theyadditionally comprise B.134 pretilachlor as further herbicide B.

Also especially preferred are compositions 64.1 to 64.3617 which differfrom the corresponding compositions 1.1 to 1.3617 only in that theyadditionally comprise B.139 2,4-D as further herbicide B.

Also especially preferred are compositions 65.1 to 65.3617 which differfrom the corresponding compositions 1.1 to 1.3617 only in that theyadditionally comprise B.146 clopyralid as further herbicide B.

Also especially preferred are compositions 66.1 to 66.3617 which differfrom the corresponding compositions 1.1 to 1.3617 only in that theyadditionally comprise B.149 dicamba as further herbicide B.

Also especially preferred are compositions 67.1 to 67.3617 which differfrom the corresponding compositions 1.1 to 1.3617 only in that theyadditionally comprise B.162 MCPA as further herbicide B.

Also especially preferred are compositions 68.1 to 68.3617 which differfrom the corresponding compositions 1.1 to 1.3617 only in that theyadditionally comprise B.165 quinclorac as further herbicide B.

Also especially preferred are compositions 69.1 to 69.3617 which differfrom the corresponding compositions 1.1 to 1.3617 only in that theyadditionally comprise B.176 indaziflam as further herbicide B.

Also especially preferred are compositions 70.1 to 70.3617 which differfrom the corresponding compositions 1.1 to 1.3383 only in that theyadditionally comprise B.2 clodinafop-propargyl as further herbicide B.

Also especially preferred are compositions 71.1 to 71.3617 which differfrom the corresponding compositions 2.1 to 2.3617 only in that theyadditionally comprise B.8 pinoxaden as further herbicide B.

Also especially preferred are compositions 72.1 to 72.3617 which differfrom the corresponding compositions 2.1 to 2.3617 only in that theyadditionally comprise B.30 imazamox as further herbicide B.

Also especially preferred are compositions 73.1 to 73.3617 which differfrom the corresponding compositions 2.1 to 2.3617 only in that theyadditionally comprise B.32 imazapic as further herbicide B.

Also especially preferred are compositions 74.1 to 74.3617 which differfrom the corresponding compositions 2.1 to 2.3617 only in that theyadditionally comprise B.35 imazapyr as further herbicide B.

Also especially preferred are compositions 75.1 to 75.3617 which differfrom the corresponding compositions 2.1 to 2.3617 only in that theyadditionally comprise B.38 imazaquin as further herbicide B.

Also especially preferred are compositions 76.1 to 76.3617 which differfrom the corresponding compositions 2.1 to 2.3617 only in that theyadditionally comprise B.40 imazethapyr as further herbicide B.

Also especially preferred are compositions 77.1 to 77.3617 which differfrom the corresponding compositions 2.1 to 2.3617 only in that theyadditionally comprise B.51 nicosulfuron as further herbicide B.

Also especially preferred are compositions 78.1 to 78.3617 which differfrom the corresponding compositions 2.1 to 2.3617 only in that theyadditionally comprise B.55 pyribenzoxim as further herbicide B.

Also especially preferred are compositions 79.1 to 79.3617 which differfrom the corresponding compositions 2.1 to 2.3617 only in that theyadditionally comprise B.56 pyriftalid as further herbicide B.

Also especially preferred are compositions 80.1 to 80.3617 which differfrom the corresponding compositions 2.1 to 2.3617 only in that theyadditionally comprise B.64 tritosulfuron as further herbicide B.

Also especially preferred are compositions 81.1 to 81.3617 which differfrom the corresponding compositions 2.1 to 2.3617 only in that theyadditionally comprise B.66 ametryne as further herbicide B.

Also especially preferred are compositions 82.1 to 82.3617 which differfrom the corresponding compositions 2.1 to 2.3617 only in that theyadditionally comprise B.67 atrazine as further herbicide B.

Also especially preferred are compositions 83.1 to 83.3617 which differfrom the corresponding compositions 2.1 to 2.3617 only in that theyadditionally comprise B.68 bentazon as further herbicide B.

Also especially preferred are compositions 84.1 to 84.3617 which differfrom the corresponding compositions 2.1 to 2.3617 only in that theyadditionally comprise B.69 bromoxynil as further herbicide B.

Also especially preferred are compositions 85.1 to 85.3617 which differfrom the corresponding compositions 2.1 to 2.3617 only in that theyadditionally comprise B.73 diuron as further herbicide B.

Also especially preferred are compositions 86.1 to 86.3617 which differfrom the corresponding compositions 2.1 to 2.3617 only in that theyadditionally comprise B.76 isoproturon as further herbicide B.

Also especially preferred are compositions 87.1 to 87.3617 which differfrom the corresponding compositions 2.1 to 2.3617 only in that theyadditionally comprise B.81 simazin as further herbicide B.

Also especially preferred are compositions 88.1 to 88.3617 which differfrom the corresponding compositions 2.1 to 2.3617 only in that theyadditionally comprise B.82 terbuthylazin as further herbicide B.

Also especially preferred are compositions 89.1 to 89.3617 which differfrom the corresponding compositions 2.1 to 2.3617 only in that theyadditionally comprise B.85 acifluorfen as further herbicide B.

Also especially preferred are compositions 90.1 to 90.3617 which differfrom the corresponding compositions 2.1 to 2.3617 only in that theyadditionally comprise B.88 flumioxazin as further herbicide B.

Also especially preferred are compositions 91.1 to 91.3617 which differfrom the corresponding compositions 2.1 to 2.3617 only in that theyadditionally comprise B.89 fomesafen as further herbicide B.

Also especially preferred are compositions 92.1 to 92.3617 which differfrom the corresponding compositions 2.1 to 2.3617 only in that theyadditionally comprise B.92 saflufenacil as further herbicide B.

Also especially preferred are compositions 93.1 to 93.3617 which differfrom the corresponding compositions 2.1 to 2.3617 only in that theyadditionally comprise B.93 sulfentrazone as further herbicide B.

Also especially preferred are compositions 94.1 to 94.3617 which differfrom the corresponding compositions 2.1 to 2.3617 only in that theyadditionally comprise B.96 benzbicyclone as further herbicide B.

Also especially preferred are compositions 95.1 to 95.3617 which differfrom the corresponding compositions 2.1 to 2.3617 only in that theyadditionally comprise B.97 clomazone as further herbicide B.

Also especially preferred are compositions 96.1 to 96.3617 which differfrom the corresponding compositions 2.1 to 2.3617 only in that theyadditionally comprise B.100 isoxaflutole as further herbicide B.

Also especially preferred are compositions 97.1 to 97.3617 which differfrom the corresponding compositions 2.1 to 2.3617 only in that theyadditionally comprise B.100 isoxaflutole and B.67 atrazine as furtherherbicides B.

Also especially preferred are compositions 98.1 to 98.3617 which differfrom the corresponding compositions 2.1 to 2.3617 only in that theyadditionally comprise B.100 isoxaflutole and B.76 isoproturon as furtherherbicides B.

Also especially preferred are compositions 99.1 to 99.3617 which differfrom the corresponding compositions 2.1 to 2.3617 only in that theyadditionally comprise B.100 isoxaflutole and B.82 terbutylazin asfurther herbicides B.

Also especially preferred are compositions 100.1 to 100.3617 whichdiffer from the corresponding compositions 2.1 to 2.3617 only in thatthey additionally comprise B.101 mesotrione as further herbicide B.

Also especially preferred are compositions 101.1 to 101.3617 whichdiffer from the corresponding compositions 2.1 to 2.3617 only in thatthey additionally comprise B.101 mesotrione and B.67 atrazine as furtherherbicides B.

Also especially preferred are compositions 102.1 to 102.3617 whichdiffer from the corresponding compositions 2.1 to 2.3617 only in thatthey additionally comprise B.101 mesotrione and B.76 isoproturon asfurther herbicides B.

Also especially preferred are compositions 103.1 to 103.3617 whichdiffer from the corresponding compositions 2.1 to 2.3617 only in thatthey additionally comprise B.101 mesotrione and B.82 terbutylazin asfurther herbicides B.

Also especially preferred are compositions 104.1 to 104.3617 whichdiffer from the corresponding compositions 2.1 to 2.3617 only in thatthey additionally comprise B.103 picolinafen as further herbicide B.

Also especially preferred are compositions 105.1 to 105.3617 whichdiffer from the corresponding compositions 2.1 to 2.3617 only in thatthey additionally comprise B.104 sulcotrione as further herbicide B.

Also especially preferred are compositions 106.1 to 106.3617 whichdiffer from the corresponding compositions 2.1 to 2.3617 only in thatthey additionally comprise B. 104 sulcotrione and B.67 atrazine asfurther herbicides B.

Also especially preferred are compositions 107.1 to 107.3617 whichdiffer from the corresponding compositions 2.1 to 2.3617 only in thatthey additionally comprise B. 104 sulcotrione and B.76 isoproturon asfurther herbicides B.

Also especially preferred are compositions 108.1 to 108.3617 whichdiffer from the corresponding compositions 2.1 to 2.3617 only in thatthey additionally comprise B. 104 sulcotrione and B.82 terbutylazin asfurther herbicides B.

Also especially preferred are compositions 109.1 to 109.3617 whichdiffer from the corresponding compositions 2.1 to 2.3617 only in thatthey additionally comprise B.106 tembotrione as further herbicide B.

Also especially preferred are compositions 110.1 to 110.3617 whichdiffer from the corresponding compositions 2.1 to 2.3617 only in thatthey additionally comprise B.107 topramezone as further herbicide B.

Also especially preferred are compositions 111.1 to 111.3617 whichdiffer from the corresponding compositions 2.1 to 2.3617 only in thatthey additionally comprise B.107 topramezone and B.67 atrazine asfurther herbicides B.

Also especially preferred are compositions 112.1 to 112.3617 whichdiffer from the corresponding compositions 2.1 to 2.3617 only in thatthey additionally comprise B.107 topramezone and B.76 isoproturon asfurther herbicides B.

Also especially preferred are compositions 113.1 to 113.3617 whichdiffer from the corresponding compositions 2.1 to 2.3617 only in thatthey additionally comprise B.107 topramezone and B.82 terbutylazin asfurther herbicides B.

Also especially preferred are compositions 114.1 to 114.3617 whichdiffer from the corresponding compositions 2.1 to 2.3617 only in thatthey additionally comprise B.112 glyphosate as further herbicide B.

Also especially preferred are compositions 115.1 to 115.3617 whichdiffer from the corresponding compositions 2.1 to 2.3617 only in thatthey additionally comprise B.112 glyphosate and B.67 atrazine as furtherherbicides B.

Also especially preferred are compositions 116.1 to 116.3617 whichdiffer from the corresponding compositions 2.1 to 2.3617 only in thatthey additionally comprise B.112 glyphosate and B.92 saflufenacil asfurther herbicides B.

Also especially preferred are compositions 117.1 to 117.3617 whichdiffer from the corresponding compositions 2.1 to 2.3617 only in thatthey additionally comprise B.112 glyphosate and B.100 isoxaflutole asfurther herbicides B.

Also especially preferred are compositions 118.1 to 118.3617 whichdiffer from the corresponding compositions 2.1 to 2.3617 only in thatthey additionally comprise B.112 glyphosate and B.124 acetochlor asfurther herbicides B.

Also especially preferred are compositions 119.1 to 119.3617 whichdiffer from the corresponding compositions 2.1 to 2.3617 only in thatthey additionally comprise B.112 glyphosate and B.101 mesotrione asfurther herbicides B.

Also especially preferred are compositions 120.1 to 120.3617 whichdiffer from the corresponding compositions 2.1 to 2.3617 only in thatthey additionally comprise B.112 glyphosate and B.104 sulcotrione asfurther herbicides B.

Also especially preferred are compositions 121.1 to 121.3617 whichdiffer from the corresponding compositions 2.1 to 2.3617 only in thatthey additionally comprise B.112 glyphosate and B.107 topramezone asfurther herbicides B.

Also especially preferred are compositions 122.1 to 122.3617 whichdiffer from the corresponding compositions 2.1 to 2.3617 only in thatthey additionally comprise B.118 glufosinate as further herbicide B.

Also especially preferred are compositions 123.1 to 123.3617 whichdiffer from the corresponding compositions 2.1 to 2.3617 only in thatthey additionally comprise B.122 pendimethalin as further herbicide B.

Also especially preferred are compositions 124.1 to 124.3617 whichdiffer from the corresponding compositions 2.1 to 2.3617 only in thatthey additionally comprise B.124 acetochlor as further herbicide B.

Also especially preferred are compositions 125.1 to 125.3617 whichdiffer from the corresponding compositions 2.1 to 2.3617 only in thatthey additionally comprise B.127 dimethenamid-P as further herbicide B.

Also especially preferred are compositions 126.1 to 126.3617 whichdiffer from the corresponding compositions 2.1 to 2.3617 only in thatthey additionally comprise B.128 fentrazamide as further herbicide B.

Also especially preferred are compositions 127.1 to 127.3617 whichdiffer from the corresponding compositions 2.1 to 2.3617 only in thatthey additionally comprise B.129 flufenacet as further herbicide B.

Also especially preferred are compositions 128.1 to 128.3617 whichdiffer from the corresponding compositions 2.1 to 2.3617 only in thatthey additionally comprise B.131 metazachlor as further herbicide B.

Also especially preferred are compositions 129.1 to 129.3617 whichdiffer from the corresponding compositions 2.1 to 2.3617 only in thatthey additionally comprise B.133 S-metolachlor as further herbicide B.

Also especially preferred are compositions 130.1 to 130.3617 whichdiffer from the corresponding compositions 12.1 to 2.3617 only in thatthey additionally comprise B.134 pretilachlor as further herbicide B.

Also especially preferred are compositions 131.1 to 132.3617 whichdiffer from the corresponding compositions 2.1 to 2.3617 only in thatthey additionally comprise B.139 2,4-D as further herbicide B.

Also especially preferred are compositions 132.1 to 132.3617 whichdiffer from the corresponding compositions 2.1 to 2.3617 only in thatthey additionally comprise B.146 clopyralid as further herbicide B.

Also especially preferred are compositions 133.1 to 133.3617 whichdiffer from the corresponding compositions 2.1 to 2.3617 only in thatthey additionally comprise B.149 dicamba as further herbicide B.

Also especially preferred are compositions 134.1 to 134.3617 whichdiffer from the corresponding compositions 2.1 to 2.3617 only in thatthey additionally comprise B.162 MCPA as further herbicide B.

Also especially preferred are compositions 135.1 to 135.3617 whichdiffer from the corresponding compositions 2.1 to 2.3617 only in thatthey additionally comprise B.165 quinclorac as further herbicide B.

Also especially preferred are compositions 136.1 to 136.3617 whichdiffer from the corresponding compositions 2.1 to 2.3617 only in thatthey additionally comprise B.176 indaziflam as further herbicide B.

Also especially preferred are compositions 137.1 to 137.3617 whichdiffer from the corresponding compositions 2.1 to 2.3383 only in thatthey additionally comprise B.2 clodinafop-propargyl as further herbicideB.

Also especially preferred are compositions 138.1 to 138.3617 whichdiffer from the corresponding compositions 3.1 to 3.3617 only in thatthey additionally comprise B.8 pinoxaden as further herbicide B.

Also especially preferred are compositions 139.1 to 139.3617 whichdiffer from the corresponding compositions 3.1 to 3.3617 only in thatthey additionally comprise B.30 imazamox as further herbicide B.

Also especially preferred are compositions 140.1 to 140.3617 whichdiffer from the corresponding compositions 3.1 to 3.3617 only in thatthey additionally comprise B.32 imazapic as further herbicide B.

Also especially preferred are compositions 141.1 to 141.3617 whichdiffer from the corresponding compositions 3.1 to 3.3617 only in thatthey additionally comprise B.35 imazapyr as further herbicide B.

Also especially preferred are compositions 142.1 to 142.3617 whichdiffer from the corresponding compositions 3.1 to 3.3617 only in thatthey additionally comprise B.38 imazaquin as further herbicide B.

Also especially preferred are compositions 143.1 to 143.3617 whichdiffer from the corresponding compositions 3.1 to 3.3617 only in thatthey additionally comprise B.40 imazethapyr as further herbicide B.

Also especially preferred are compositions 144.1 to 144.3617 whichdiffer from the corresponding compositions 3.1 to 3.3617 only in thatthey additionally comprise B.51 nicosulfuron as further herbicide B.

Also especially preferred are compositions 145.1 to 145.3617 whichdiffer from the corresponding compositions 3.1 to 3.3617 only in thatthey additionally comprise B.55 pyribenzoxim as further herbicide B.

Also especially preferred are compositions 146.1 to 146.3617 whichdiffer from the corresponding compositions 3.1 to 3.3617 only in thatthey additionally comprise B.56 pyriftalid as further herbicide B.

Also especially preferred are compositions 147.1 to 147.3617 whichdiffer from the corresponding compositions 3.1 to 3.3617 only in thatthey additionally comprise B.64 tritosulfuron as further herbicide B.

Also especially preferred are compositions 148.1 to 148.3617 whichdiffer from the corresponding compositions 3.1 to 3.3617 only in thatthey additionally comprise B.66 ametryne as further herbicide B.

Also especially preferred are compositions 149.1 to 149.3617 whichdiffer from the corresponding compositions 3.1 to 3.3617 only in thatthey additionally comprise B.67 atrazine as further herbicide B.

Also especially preferred are compositions 150.1 to 150.3617 whichdiffer from the corresponding compositions 3.1 to 3.3617 only in thatthey additionally comprise B.68 bentazon as further herbicide B.

Also especially preferred are compositions 151.1 to 151.3617 whichdiffer from the corresponding compositions 3.1 to 3.3617 only in thatthey additionally comprise B.69 bromoxynil as further herbicide B.

Also especially preferred are compositions 152.1 to 152.3617 whichdiffer from the corresponding compositions 3.1 to 3.3617 only in thatthey additionally comprise B.73 diuron as further herbicide B.

Also especially preferred are compositions 153.1 to 153.3617 whichdiffer from the corresponding compositions 3.1 to 3.3617 only in thatthey additionally comprise B.76 isoproturon as further herbicide B.

Also especially preferred are compositions 154.1 to 154.3617 whichdiffer from the corresponding compositions 3.1 to 3.3617 only in thatthey additionally comprise B.81 simazin as further herbicide B.

Also especially preferred are compositions 155.1 to 155.3617 whichdiffer from the corresponding compositions 3.1 to 3.3617 only in thatthey additionally comprise B.82 terbuthylazin as further herbicide B.

Also especially preferred are compositions 156.1 to 156.3617 whichdiffer from the corresponding compositions 3.1 to 3.3617 only in thatthey additionally comprise B.85 acifluorfen as further herbicide B.

Also especially preferred are compositions 157.1 to 157.3617 whichdiffer from the corresponding compositions 3.1 to 3.3617 only in thatthey additionally comprise B.88 flumioxazin as further herbicide B.

Also especially preferred are compositions 158.1 to 158.3617 whichdiffer from the corresponding compositions 3.1 to 3.3617 only in thatthey additionally comprise B.89 fomesafen as further herbicide B.

Also especially preferred are compositions 159.1 to 159.3617 whichdiffer from the corresponding compositions 3.1 to 3.3617 only in thatthey additionally comprise B.92 saflufenacil as further herbicide B.

Also especially preferred are compositions 160.1 to 160.3617 whichdiffer from the corresponding compositions 3.1 to 3.3617 only in thatthey additionally comprise B.93 sulfentrazone as further herbicide B.

Also especially preferred are compositions 161.1 to 161.3617 whichdiffer from the corresponding compositions 3.1 to 3.3617 only in thatthey additionally comprise B.96 benzbicyclone as further herbicide B.

Also especially preferred are compositions 162.1 to 162.3617 whichdiffer from the corresponding compositions 3.1 to 3.3617 only in thatthey additionally comprise B.97 clomazone as further herbicide B.

Also especially preferred are compositions 163.1 to 163.3617 whichdiffer from the corresponding compositions 3.1 to 3.3617 only in thatthey additionally comprise B.100 isoxaflutole as further herbicide B.

Also especially preferred are compositions 164.1 to 164.3617 whichdiffer from the corresponding compositions 3.1 to 3.3617 only in thatthey additionally comprise B.100 isoxaflutole and B.67 atrazine asfurther herbicides B.

Also especially preferred are compositions 165.1 to 165.3617 whichdiffer from the corresponding compositions 3.1 to 3.3617 only in thatthey additionally comprise B.100 isoxaflutole and B.76 isoproturon asfurther herbicides B.

Also especially preferred are compositions 166.1 to 166.3617 whichdiffer from the corresponding compositions 3.1 to 3.3617 only in thatthey additionally comprise B.100 isoxaflutole and B.82 terbutylazin asfurther herbicides B.

Also especially preferred are compositions 167.1 to 167.3617 whichdiffer from the corresponding compositions 3.1 to 3.3617 only in thatthey additionally comprise B.101 mesotrione as further herbicide B.

Also especially preferred are compositions 168.1 to 168.3617 whichdiffer from the corresponding compositions 3.1 to 3.3617 only in thatthey additionally comprise B.101 mesotrione and B.67 atrazine as furtherherbicides B.

Also especially preferred are compositions 169.1 to 169.3617 whichdiffer from the corresponding compositions 3.1 to 3.3617 only in thatthey additionally comprise B.101 mesotrione and B.76 isoproturon asfurther herbicides B.

Also especially preferred are compositions 170.1 to 170.3617 whichdiffer from the corresponding compositions 3.1 to 3.3617 only in thatthey additionally comprise B.101 mesotrione and B.82 terbutylazin asfurther herbicides B.

Also especially preferred are compositions 171.1 to 171.3617 whichdiffer from the corresponding compositions 3.1 to 3.3617 only in thatthey additionally comprise B.103 picolinafen as further herbicide B.

Also especially preferred are compositions 172.1 to 172.3617 whichdiffer from the corresponding compositions 3.1 to 3.3617 only in thatthey additionally comprise B.104 sulcotrione as further herbicide B.

Also especially preferred are compositions 173.1 to 173.3617 whichdiffer from the corresponding compositions 3.1 to 3.3617 only in thatthey additionally comprise B. 104 sulcotrione and B.67 atrazine asfurther herbicides B.

Also especially preferred are compositions 174.1 to 174.3617 whichdiffer from the corresponding compositions 3.1 to 3.3617 only in thatthey additionally comprise B. 104 sulcotrione and B.76 isoproturon asfurther herbicides B.

Also especially preferred are compositions 175.1 to 175.3617 whichdiffer from the corresponding compositions 3.1 to 3.3617 only in thatthey additionally comprise B. 104 sulcotrione and B.82 terbutylazin asfurther herbicides B.

Also especially preferred are compositions 176.1 to 176.3617 whichdiffer from the corresponding compositions 3.1 to 3.3617 only in thatthey additionally comprise B.106 tembotrione as further herbicide B.

Also especially preferred are compositions 177.1 to 177.3617 whichdiffer from the corresponding compositions 3.1 to 3.3617 only in thatthey additionally comprise B.107 topramezone as further herbicide B.

Also especially preferred are compositions 178.1 to 178.3617 whichdiffer from the corresponding compositions 3.1 to 3.3617 only in thatthey additionally comprise B.107 topramezone and B.67 atrazine asfurther herbicides B.

Also especially preferred are compositions 179.1 to 179.3617 whichdiffer from the corresponding compositions 3.1 to 3.3617 only in thatthey additionally comprise B.107 topramezone and B.76 isoproturon asfurther herbicides B.

Also especially preferred are compositions 180.1 to 180.3617 whichdiffer from the corresponding compositions 3.1 to 3.3617 only in thatthey additionally comprise B.107 topramezone and B.82 terbutylazin asfurther herbicides B.

Also especially preferred are compositions 181.1 to 181.3617 whichdiffer from the corresponding compositions 3.1 to 3.3617 only in thatthey additionally comprise B.112 glyphosate as further herbicide B.

Also especially preferred are compositions 182.1 to 182.3617 whichdiffer from the corresponding compositions 3.1 to 3.3617 only in thatthey additionally comprise B.112 glyphosate and B.67 atrazine as furtherherbicides B.

Also especially preferred are compositions 183.1 to 183.3617 whichdiffer from the corresponding compositions 3.1 to 3.3617 only in thatthey additionally comprise B.112 glyphosate and B.92 saflufenacil asfurther herbicides B.

Also especially preferred are compositions 184.1 to 184.3617 whichdiffer from the corresponding compositions 3.1 to 3.3617 only in thatthey additionally comprise B.112 glyphosate and B.100 isoxaflutole asfurther herbicides B.

Also especially preferred are compositions 185.1 to 185.3617 whichdiffer from the corresponding compositions 3.1 to 3.3617 only in thatthey additionally comprise B.112 glyphosate and B.124 acetochlor asfurther herbicides B.

Also especially preferred are compositions 186.1 to 186.3617 whichdiffer from the corresponding compositions 3.1 to 3.3617 only in thatthey additionally comprise B.112 glyphosate and B.101 mesotrione asfurther herbicides B.

Also especially preferred are compositions 187.1 to 187.3617 whichdiffer from the corresponding compositions 3.1 to 3.3617 only in thatthey additionally comprise B.112 glyphosate and B.104 sulcotrione asfurther herbicides B.

Also especially preferred are compositions 188.1 to 188.3617 whichdiffer from the corresponding compositions 3.1 to 3.3617 only in thatthey additionally comprise B.112 glyphosate and B.107 topramezone asfurther herbicides B.

Also especially preferred are compositions 189.1 to 189.3617 whichdiffer from the corresponding compositions 3.1 to 3.3617 only in thatthey additionally comprise B.118 glufosinate as further herbicide B.

Also especially preferred are compositions 190.1 to 190.3617 whichdiffer from the corresponding compositions 3.1 to 3.3617 only in thatthey additionally comprise B.122 pendimethalin as further herbicide B.

Also especially preferred are compositions 191.1 to 191.3617 whichdiffer from the corresponding compositions 3.1 to 3.3617 only in thatthey additionally comprise B.124 acetochlor as further herbicide B.

Also especially preferred are compositions 192.1 to 192.3617 whichdiffer from the corresponding compositions 3.1 to 3.3617 only in thatthey additionally comprise B.127 dimethenamid-P as further herbicide B.

Also especially preferred are compositions 193.1 to 193.3617 whichdiffer from the corresponding compositions 3.1 to 3.3617 only in thatthey additionally comprise B.128 fentrazamide as further herbicide B.

Also especially preferred are compositions 194.1 to 194.3617 whichdiffer from the corresponding compositions 3.1 to 3.3617 only in thatthey additionally comprise B.129 flufenacet as further herbicide B.

Also especially preferred are compositions 195.1 to 195.3617 whichdiffer from the corresponding compositions 3.1 to 3.3617 only in thatthey additionally comprise B.131 metazachlor as further herbicide B.

Also especially preferred are compositions 196.1 to 196.3617 whichdiffer from the corresponding compositions 3.1 to 3.3617 only in thatthey additionally comprise B.133 S-metolachlor as further herbicide B.

Also especially preferred are compositions 197.1 to 197.3617 whichdiffer from the corresponding compositions 13.1 to 3.3617 only in thatthey additionally comprise B.134 pretilachlor as further herbicide B.

Also especially preferred are compositions 198.1 to 198.3617 whichdiffer from the corresponding compositions 3.1 to 3.3617 only in thatthey additionally comprise B.139 2,4-D as further herbicide B.

Also especially preferred are compositions 199.1 to 199.3617 whichdiffer from the corresponding compositions 3.1 to 3.3617 only in thatthey additionally comprise B.146 clopyralid as further herbicide B.

Also especially preferred are compositions 200.1 to 200.3617 whichdiffer from the corresponding compositions 3.1 to 3.3617 only in thatthey additionally comprise B.149 dicamba as further herbicide B.

Also especially preferred are compositions 201.1 to 201.3617 whichdiffer from the corresponding compositions 3.1 to 3.3617 only in thatthey additionally comprise B.162 MCPA as further herbicide B.

Also especially preferred are compositions 202.1 to 202.3617 whichdiffer from the corresponding compositions 3.1 to 3.3617 only in thatthey additionally comprise B.165 quinclorac as further herbicide B.

Also especially preferred are compositions 203.1 to 203.3617 whichdiffer from the corresponding compositions 3.1 to 3.3617 only in thatthey additionally comprise B.176 indaziflam as further herbicide B.

Also especially preferred are compositions 204.1 to 204.3617 whichdiffer from the corresponding compositions 3.1 to 3.3383 only in thatthey additionally comprise B.2 clodinafop-propargyl as further herbicideB.

The invention also relates to agrochemical compositions comprising anauxiliary and a composition according to the invention.

An agrochemical composition comprises a pesticidally effective amount ofat least one composition according to the invention. The term “effectiveamount” denotes an amount of the active ingredients, which is sufficientfor controlling unwanted plants, especially for controlling unwantedplants in cultivated plants and which does not result in a substantialdamage to the treated plants. Such an amount can vary in a broad rangeand is dependent on various factors, such as the plants to becontrolled, the treated cultivated plant or material, the climaticconditions and the specific composition according to the invention used.

The compounds A and optionally B and/or C, their N-oxides, salts orderivatives can be converted into customary types of agrochemicalcompositions, e.g. solutions, emulsions, suspensions, dusts, powders,pastes, granules, pressings, capsules, and mixtures thereof. Examplesfor agrochemical composition types are suspensions (e.g. SC, OD, FS),emulsifiable concentrates (e.g. EC), emulsions (e.g. EW, EO, ES, ME),capsules (e.g. CS, ZC), pastes, pastilles, wettable powders or dusts(e.g. WP, SP, WS, DP, DS), pressings (e.g. BR, TB, DT), granules (e.g.WG, SG, GR, FG, GG, MG), insecticidal articles (e.g. LN), as well as gelformulations for the treatment of plant propagation materials such asseeds (e.g. GF). These and further agrochemical compositions types aredefined in the “Catalogue of pesticide formulation types andinternational coding system”, Technical Monograph No. 2, 6^(th) Ed. May2008, CropLife International.

The agrochemical compositions are prepared in a known manner, such asdescribed by Mollet and Grubemann, Formulation technology, Wiley VCH,Weinheim, 2001; or Knowles, New developments in crop protection productformulation, Agrow Reports DS243, T&F Informa, London, 2005.

Suitable auxiliaries are solvents, liquid carriers, solid carriers orfillers, surfactants, dispersants, emulsifiers, wetters, adjuvants,solubilizers, penetration enhancers, protective colloids, adhesionagents, thickeners, humectants, repellents, attractants, feedingstimulants, compatibilizers, bactericides, anti-freezing agents,anti-foaming agents, colorants, tackifiers and binders.

Suitable solvents and liquid carriers are water and organic solvents,such as mineral oil fractions of medium to high boiling point, e.g.kerosene, diesel oil; oils of vegetable or animal origin; aliphatic,cyclic and aromatic hydrocarbons, e.g. toluene, paraffin,tetrahydronaphthalene, alkylated naphthalenes; alcohols, e.g. ethanol,propanol, butanol, benzylalcohol, cyclohexanol; glycols; DMSO; ketones,e.g. cyclohexanone; esters, e.g. lactates, carbonates, fatty acidesters, gamma-butyrolactone; fatty acids; phosphonates; amines; amides,e.g. N-methylpyrrolidone, fatty acid dimethylamides; and mixturesthereof.

Suitable solid carriers or fillers are mineral earths, e.g. silicates,silica gels, talc, kaolins, limestone, lime, chalk, clays, dolomite,diatomaceous earth, bentonite, calcium sulfate, magnesium sulfate,magnesium oxide; polysaccharides, e.g. cellulose, starch; fertilizers,e.g. ammonium sulfate, ammonium phosphate, ammonium nitrate, ureas;products of vegetable origin, e.g. cereal meal, tree bark meal, woodmeal, nutshell meal, and mixtures thereof.

Suitable surfactants are surface-active compounds, such as anionic,cationic, nonionic and amphoteric surfactants, block polymers,polyelectrolytes, and mixtures thereof. Such surfactants can be used asemulsifier, dispersant, solubilizer, wetter, penetration enhancer,protective colloid, or adjuvant. Examples of surfactants are listed inMcCutcheon's, Vol. 1: Emulsifiers & Detergents, McCutcheon'sDirectories, Glen Rock, USA, 2008 (International Ed. or North AmericanEd.).

Suitable anionic surfactants are alkali, alkaline earth or ammoniumsalts of sulfonates, sulfates, phosphates, carboxylates, and mixturesthereof. Examples of sulfonates are alkylarylsulfonates,diphenylsulfonates, alpha-olefin sulfonates, lignine sulfonates,sulfonates of fatty acids and oils, sulfonates of ethoxylatedalkylphenols, sulfonates of alkoxylated arylphenols, sulfonates ofcondensed naphthalenes, sulfonates of dodecyl- and tridecylbenzenes,sulfonates of naphthalenes and alkylnaphthalenes, sulfosuccinates orsulfosuccinamates. Examples of sulfates are sulfates of fatty acids andoils, of ethoxylated alkylphenols, of alcohols, of ethoxylated alcohols,or of fatty acid esters. Examples of phosphates are phosphate esters.Examples of carboxylates are alkyl carboxylates, and carboxylatedalcohol or alkylphenol ethoxylates.

Suitable nonionic surfactants are alkoxylates, N-substituted fatty acidamides, amine oxides, esters, sugar-based surfactants, polymericsurfactants, and mixtures thereof. Examples of alkoxylates are compoundssuch as alcohols, alkylphenols, amines, amides, arylphenols, fatty acidsor fatty acid esters which have been alkoxylated with 1 to 50equivalents. Ethylene oxide and/or propylene oxide may be employed forthe alkoxylation, preferably ethylene oxide. Examples of N-substitutedfatty acid amides are fatty acid glucamides or fatty acid alkanolamides.Examples of esters are fatty acid esters, glycerol esters ormonoglycerides. Examples of sugar-based surfactants are sorbitans,ethoxylated sorbitans, sucrose and glucose esters oralkylpolyglucosides. Examples of polymeric surfactants are home- orcopolymers of vinylpyrrolidone, vinylalcohols, or vinylacetate.

Suitable cationic surfactants are quaternary surfactants, for examplequaternary ammonium compounds with one or two hydrophobic groups, orsalts of long-chain primary amines. Suitable amphoteric surfactants arealkylbetains and imidazolines. Suitable block polymers are blockpolymers of the A-B or A-B-A type comprising blocks of polyethyleneoxide and polypropylene oxide, or of the A-B-C type comprising alkanol,polyethylene oxide and polypropylene oxide. Suitable polyelectrolytesare polyacids or polybases. Examples of polyacids are alkali salts ofpolyacrylic acid or polyacid comb polymers. Examples of polybases arepolyvinylamines or polyethyleneamines.

Suitable adjuvants are compounds, which have a neglectable or even nopesticidal activity themselves, and which improve the biologicalperformance of the compound I on the target. Examples are surfactants,mineral or vegetable oils, and other auxiliaries. Further examples arelisted by Knowles, Adjuvants and additives, Agrow Reports DS256, T&FInforma UK, 2006, chapter 5.

Suitable thickeners are polysaccharides (e.g. xanthan gum,carboxymethylcellulose), inorganic clays (organically modified orunmodified), polycarboxylates, and silicates.

Suitable bactericides are bronopol and isothiazolinone derivatives suchas alkylisothiazolinones and benzisothiazolinones.

Suitable anti-freezing agents are ethylene glycol, propylene glycol,urea and glycerin.

Suitable anti-foaming agents are silicones, long chain alcohols, andsalts of fatty acids.

Suitable colorants (e.g. in red, blue, or green) are pigments of lowwater solubility and water-soluble dyes. Examples are inorganiccolorants (e.g. iron oxide, titan oxide, iron hexacyanoferrate) andorganic colorants (e.g. alizarin-, azo- and phthalocyanine colorants).

Suitable tackifiers or binders are polyvinylpyrrolidons,polyvinylacetates, polyvinyl alcohols, polyacrylates, biological orsynthetic waxes, and cellulose ethers.

Examples for agrochemical composition types and their preparation are:

i) Water-Soluble Concentrates (SL, LS)

10-60 wt % of a compostion according to the invention and 5-15 wt %wetting agent (e.g. alcohol alkoxylates) are dissolved in water and/orin a water-soluble solvent (e.g. alcohols) ad 100 wt %. The activesubstance dissolves upon dilution with water.

ii) Dispersible Concentrates (DC)

5-25 wt % of a composition according to the invention and 1-10 wt %dispersant (e.g. polyvinylpyrrolidone) are dissolved in organic solvent(e.g. cyclohexanone) ad 100 wt %. Dilution with water gives adispersion.

iii) Emulsifiable Concentrates (EC)

15-70 wt % of a composition according to the invention and 5-10 wt %emulsifiers (e.g. calcium dodecylbenzenesulfonate and castor oilethoxylate) are dissolved in water-insoluble organic solvent (e.g.aromatic hydrocarbon) ad 100 wt %. Dilution with water gives anemulsion.

iv) Emulsions (EW, EO, ES)

5-40 wt % of a composition according to the invention and 1-10 wt %emulsifiers (e.g. calcium dodecylbenzenesulfonate and castor oilethoxylate) are dissolved in 20-40 wt % water-insoluble organic solvent(e.g. aromatic hydrocarbon). This mixture is introduced into water ad100 wt % by means of an emulsifying machine and made into a homogeneousemulsion. Dilution with water gives an emulsion.

v) Suspensions (SC, OD, FS)

In an agitated ball mill, 20-60 wt % of a composition according to theinvention are comminuted with addition of 2-10 wt % dispersants andwetting agents (e.g. sodium lignosulfonate and alcohol ethoxylate),0.1-2 wt % thickener (e.g. xanthan gum) and water ad 100 wt % to give afine active substance suspension. Dilution with water gives a stablesuspension of the active substance. For FS type composition up to 40 wt% binder (e.g. polyvinylalcohol) is added.

vi) Water-Dispersible Granules and Water-Soluble Granules (WG, SG)

50-80 wt % of a composition according to the invention are ground finelywith addition of dispersants and wetting agents (e.g. sodiumlignosulfonate and alcohol ethoxylate) ad 100 wt % and prepared aswater-dispersible or water-soluble granules by means of technicalappliances (e.g. extrusion, spray tower, fluidized bed). Dilution withwater gives a stable dispersion or solution of the active substance.

vii) Water-Dispersible Powders and Water-Soluble Powders (WP, SP, WS)

50-80 wt % of a composition according to the invention are ground in arotor-stator mill with addition of 1-5 wt % dispersants (e.g. sodiumlignosulfonate), 1-3 wt % wetting agents (e.g. alcohol ethoxylate) andsolid carrier (e.g. silica gel) ad 100 wt %. Dilution with water gives astable dispersion or solution of the active substance.

viii) Gel (GW, GF)

In an agitated ball mill, 5-25 wt % of a composition according to theinvention are comminuted with addition of 3-10 wt % dispersants (e.g.sodium lignosulfonate), 1-5 wt % thickener (e.g. carboxymethylcellulose)and water ad 100 wt % to give a fine suspension of the active substance.Dilution with water gives a stable suspension of the active substance.

ix) Microemulsion (ME)

5-20 wt % of a composition according to the invention are added to 5-30wt % organic solvent blend (e.g. fatty acid dimethylamide andcyclohexanone), 10-25 wt % surfactant blend (e.g. alcohol ethoxylate andarylphenol ethoxylate), and water ad 100%. This mixture is stirred for 1h to produce spontaneously a thermodynamically stable microemulsion.

x) Microcapsules (CS)

An oil phase comprising 5-50 wt % of a composition according to theinvention, 0-40 wt % water insoluble organic solvent (e.g. aromatichydrocarbon), 2-15 wt % acrylic monomers (e.g. methylmethacrylate,methacrylic acid and a di- or triacrylate) are dispersed into an aqueoussolution of a protective colloid (e.g. polyvinyl alcohol). Radicalpolymerization initiated by a radical initiator results in the formationof poly(meth)acrylate microcapsules. Alternatively, an oil phasecomprising 5-50 wt % of a compound I according to the invention, 0-40 wt% water insoluble organic solvent (e.g. aromatic hydrocarbon), and anisocyanate monomer (e.g. diphenylmethene-4,4′-diisocyanate) aredispersed into an aqueous solution of a protective colloid (e.g.polyvinyl alcohol). The addition of a polyamine (e.g.hexamethylenediamine) results in the formation of polyureamicrocapsules. The monomers amount to 1-10 wt %. The wt % relate to thetotal CS composition.

xi) Dustable Powders (DP, DS)

1-10 wt % of a composition according to the invention are ground finelyand mixed intimately with solid carrier (e.g. finely divided kaolin) ad100 wt %.

xii) Granules (GR, FG)

0.5-30 wt % of a composition according to the invention is ground finelyand associated with solid carrier (e.g. silicate) ad 100 wt %.Granulation is achieved by extrusion, spray-drying or the fluidized bed.

xiii) Ultra-Low Volume Liquids (UL)

1-50 wt % of a composition according to the invention are dissolved inorganic solvent (e.g. aromatic hydrocarbon) ad 100 wt %.

The agrochemical composition types i) to xiii) may optionally comprisefurther auxiliaries, such as 0.1-1 wt % bactericides, 5-15 wt %anti-freezing agents, 0.1-1 wt % anti-foaming agents, and 0.1-1 wt %colorants.

The agrochemical compositions generally comprise between 0.01 and 95%,preferably between 0.1 and 90%, and in particular between 0.5 and 75%,by weight of active substance. The active substances are employed in apurity of from 90% to 100%, preferably from 95% to 100% (according toNMR spectrum).

Solutions for seed treatment (LS), suspoemulsions (SE), flowableconcentrates (FS), powders for dry treatment (DS), water-dispersiblepowders for slurry treatment (WS), water-soluble powders (SS), emulsions(ES), emulsifiable concentrates (EC) and gels (GF) are usually employedfor the purposes of treatment of plant propagation materials,particularly seeds. The compositions in question give, aftertwo-to-tenfold dilution, active substance concentrations of from 0.01 to60% by weight, preferably from 0.1 to 40% by weight, in the ready-to-usepreparations. Application can be carried out before or during sowing.

Methods for applying compounds of formula (I) and compositionscomprising them, respectively, on to plant propagation material,especially seeds include dressing, coating, pelleting, dusting, soakingand in-furrow application methods of the propagation material.Preferably, compound I or the compositions thereof, respectively, areapplied on to the plant propagation material by a method such thatgermination is not induced, e.g. by seed dressing, pelleting, coatingand dusting.

Various types of oils, wetters, adjuvants, fertilizer, ormicronutrients, and further pesticides (e.g. herbicides, insecticides,fungicides, growth regulators, safeners) may be added to the activesubstances or the compositions comprising them as premix or, ifappropriate not until immediately prior to use (tank mix). These agentscan be admixed with the compositions according to the invention in aweight ratio of 1:100 to 100:1, preferably 1:10 to 10:1.

The user applies the agrochemical composition according to the inventionusually from a predosage device, a knapsack sprayer, a spray tank, aspray plane, or an irrigation system. Usually, the agrochemicalcomposition is made up with water, buffer, and/or further auxiliaries tothe desired application concentration and the ready-to-use spray liquoror the agrochemical composition according to the invention is thusobtained. Usually, 20 to 2000 liters, preferably 50 to 400 liters, ofthe ready-to-use spray liquor are applied per hectare of agriculturaluseful area.

According to one embodiment, either individual components of theagrochemical composition according to the invention or partiallypremixed components, e.g. agrochemical components comprising anisoxazolo[5,4-b]pyridine of formula (I) and/or active substances fromthe groups B and/or C may be mixed by the user in a spray tank andfurther auxiliaries and additives may be added, if appropriate.

In a further embodiment, individual components of the agrochemicalcomposition according to the invention such as parts of a kit or partsof a binary or ternary mixture may be mixed by the user himself in aspray tank and further auxiliaries may be added, if appropriate.

In a further embodiment, either individual components of theagrochemical composition according to the invention or partiallypremixed components, e.g. components comprising anisoxazolo[5,4-b]pyridine of formula (I) and active substances from thegroups B and/or C, can be applied jointly (e.g. after tank mix) orconsecutively.

Accordingly, a first embodiment of the invention relates to compositionsin the form of an agrochemical composition formulated as a 1-componentcomposition comprising the at least one isoxazolo[5,4-b]pyridine offormula (I) (component A) and as component B at least one further activecompound selected from the herbicides B, and, if desired, the safeners Cand also a solid or liquid carrier and, if appropriate, one or moresurfactants.

Accordingly, a second embodiment of the invention relates tocompositions in the form of a agrochemical composition formulated as a2-component composition comprising a first formulation (component)comprising the at least one isoxazolo[5,4-b]pyridine of formula (I)(component A), a solid or liquid carrier and, if appropriate, one ormore surfactants, and as component B at least one further herbicide Band safeners C, a solid or liquid carrier and, if appropriate, one ormore surfactants.

The isoxazolo[5,4-b]pyridine of formula (I) (component A) and the atleast one further active herbicide B (component B) and/or C can beformulated and applied jointly or separately, simultaneously or insuccession, before, during or after the emergence of the plants. In caseof separate application, the order of the application of the componentsA, B and/or C is of minor importance. The only thing that is importantis that the at least one isoxazolo[5,4-b]pyridine of formula (I) and theat least one further herbicide B and/or C are present simultaneously atthe site of action, i.e. are at the same time in contact with or takenup by the plant to be controlled.

The compositions according to the invention are suitable as herbicides.They are suitable as such or as an appropriately formulated composition(agrochemical composition).

The compositions according to the invention control vegetation onnon-crop areas very efficiently, especially at high rates ofapplication. They act against broad-leafed weeds and grass weeds incrops such as wheat, rice, corn, soybeans and cotton without causing anysignificant damage to the crop plants. This effect is mainly observed atlow rates of application.

The compositions according to the invention are applied to the plantsmainly by spraying the leaves. Here, the application can be carried outusing, for example, water as carrier by customary spraying techniquesusing spray liquor amounts of from about 100 to 1000 I/ha (for examplefrom 300 to 400 I/ha). The herbicidal compositions may also be appliedby the low-volume or the ultra-low-volume method, or in the form ofmicrogranules.

Application of the herbicidal compositions according to the presentinvention can be done before, during and/or after, preferably duringand/or after, the emergence of the undesirable plants.

The herbicidal compositions according to the present invention can beapplied pre- or post-emergence or together with the seed of a cropplant. It is also possible to apply the compounds and compositions byapplying seed, pretreated with a composition of the invention, of a cropplant. If the active components A and B, and, if appropriate, C, areless well tolerated by certain crop plants, application techniques maybe used in which the herbicidal compositions are sprayed, with the aidof the spraying equipment, in such a way that as far as possible they donot come into contact with the leaves of the sensitive crop plants,while the active compounds reach the leaves of undesirable plantsgrowing underneath, or the bare soil surface (post-directed, lay-by).

In a further embodiment, the composition according to the invention canbe applied by treating seed. The treatment of seed comprises essentiallyall procedures familiar to the person skilled in the art (seed dressing,seed coating, seed dusting, seed soaking, seed film coating, seedmultilayer coating, seed encrusting, seed dripping and seed pelleting)based on the isoxazolo[5,4-b]pyridine of formula (I) according to theinvention or the compositions prepared therefrom. Here, the herbicidalcompositions can be applied diluted or undiluted.

The term “seed” comprises seed of all types, such as, for example,corns, seeds, fruits, tubers, seedlings and similar forms. Here,preferably, the term seed describes corns and seeds. The seed used canbe seed of the useful plants mentioned above, but also the seed oftransgenic plants or plants obtained by customary breeding methods.

Moreover, it may be advantageous to apply the compositions of thepresent invention on their own or jointly in combination with other cropprotection agents, for example with agents for controlling pests orphytopathogenic fungi or bacteria or with groups of active compoundswhich regulate growth. Also of interest is the miscibility with mineralsalt solutions which are employed for treating nutritional and traceelement deficiencies. Non-phytotoxic oils and oil concentrates can alsobe added.

When employed in plant protection, the amounts of active substancesapplied, i.e. components A and B, and, if appropriate, C, withoutformulation auxiliaries, are, depending on the kind of effect desired,from 0.001 to 3 kg/ha, preferably from 0.005 to 2.5 kg/ha and inparticular from 0.01 to 2 kg/ha of active substance (a.s.).

In another preferred embodiment of the invention, the rates ofapplication of the isoxazolo[5,4-b]pyridine of formula (I) according tothe present invention (total amount of isoxazolo[5,4-b]pyridine offormula (I)) are from 0.1 g/ha to 3000 g/ha, preferably 10 g/ha to 1000g/ha, depending on the control target, the season, the target plants andthe growth stage.

In another preferred embodiment of the invention, the application ratesof the isoxazolo[5,4-b]pyridine of formula (I) are in the range from 0.1g/ha to 5000 g/ha and preferably in the range from 1 g/ha to 2500 g/haor from 5 g/ha to 2000 g/ha.

In another preferred embodiment of the invention, the application rateof the isoxazolo[5,4-b]pyridine of formula (I) is 0.1 to 1000 g/ha,preferably 1 to 750 g/ha, more preferably 5 to 500 g/ha.

The required application rates of herbicides B are generally in therange of from 0.0005 kg/ha to 2.5 kg/ha and preferably in the range offrom 0.005 kg/ha to 2 kg/ha or 0.01 kg/ha to 1.5 kg/h of a.s.

The required application rates of safeners C are generally in the rangeof from 0.0005 kg/ha to 2.5 kg/ha and preferably in the range of from0.005 kg/ha to 2 kg/ha or 0.01 kg/ha to 1.5 kg/h of a.s.

In treatment of plant propagation materials such as seeds, e.g. bydusting, coating or drenching seed, amounts of active substance of from0.1 to 1000 g, preferably from 1 to 1000 g, more preferably from 1 to100 g and most preferably from 5 to 100 g, per 100 kilogram of plantpropagation material (preferably seeds) are generally required.

In another embodiment of the invention, to treat the seed, the amountsof composition components applied, i.e. A and B, and, if appropriate, C,are generally employed in amounts of from 0.001 to 10 kg per 100 kg ofseed.

When used in the protection of materials or stored products, the amountof composition components applied depends on the kind of applicationarea and on the desired effect. Amounts customarily applied in theprotection of materials are 0.001 g to 2 kg, preferably 0.005 g to 1 kg,of active substance per cubic meter of treated material.

In the methods of the present invention it is immaterial whether theisoxazolo[5,4-b]pyridine of formula (I), and the further herbicide Band/or the safener C are formulated and applied jointly or separately.

In the case of separate application it is of minor importance, in whichorder the application takes place. It is only necessary, that theisoxazolo[5,4-b]pyridine of formula (I) and the herbicide B and/or theherbicide safener C are applied in a time frame that allows simultaneousaction of the active ingredients on the plants, preferably within atime-frame of at most 14 days, in particular at most 7 days.

Depending on the application method in question, the compositionsaccording to the invention can additionally be employed in a furthernumber of crop plants for eliminating undesirable plants. Examples ofsuitable crops are the following:

Allium cepa, Ananas comosus, Arachis hypogaea, Asparagus officinalis,Avena sativa, Beta vulgaris spec. altissima, Beta vulgaris spec. rapa,Brassica napus var. napus, Brassica napus var. napobrassica, Brassicarapa var. silvestris, Brassica oleracea, Brassica nigra, Camelliasinensis, Carthamus tinctorius, Carya illinoinensis, Citrus limon,Citrus sinensis, Coffea arabica (Coffea canephora, Coffea liberica),Cucumis sativus, Cynodon dactylon, Daucus carota, Elaeis guineensis,Fragaria vesca, Glycine max, Gossypium hirsutum, (Gossypium arboreum,Gossypium herbaceum, Gossypium vitifolium), Helianthus annuus, Heveabrasiliensis, Hordeum vulgare, Humulus lupulus, Ipomoea batatas, Juglansregia, Lens culinaris, Linum usitatissimum, Lycopersicon lycopersicum,Malus spec., Manihot esculenta, Medicago sativa, Musa spec., Nicotianatabacum (N. rustica), Olea europaea, Oryza sativa, Phaseolus lunatus,Phaseolus vulgaris, Picea abies, Pinus spec., Pistacia vera, Pisumsativum, Prunus avium, Prunus persica, Pyrus communis, Prunus armeniaca,Prunus cerasus, Prunus dulcis and prunus domestica, Ribes sylvestre,Ricinus communis, Saccharum officinarum, Secale cereale, Sinapis alba,Solanum tuberosum, Sorghum bicolor (S. vulgare), Theobroma cacao,Trifolium pratense, Triticum aestivum, Triticale, Triticum durum, Viciafaba, Vitis vinifera, Zea mays.

Preferred crops are Arachis hypogaea, Beta vulgaris spec. altissima,Brassica napus var. napus, Brassica oleracea, Citrus limon, Citrussinensis, Coffea arabica (Coffea canephora, Coffea liberica), Cynodondactylon, Glycine max, Gossypium hirsutum, (Gossypium arboreum,Gossypium herbaceum, Gossypium vitifolium), Helianthus annuus, Hordeumvulgare, Juglans regia, Lens culinaris, Linum usitatissimum,Lycopersicon lycopersicum, Malus spec., Medicago sativa, Nicotianatabacum (N. rustica), Olea europaea, Oryza sativa , Phaseolus lunatus,Phaseolus vulgaris, Pistacia vera, Pisum sativum, Prunus dulcis,Saccharum officinarum, Secale cereale, Solanum tuberosum, Sorghumbicolor (S. vulgare), Triticale, Triticum aestivum, Triticum durum,Vicia faba, Vitis vinifera and Zea mays

Especially preferred crops are crops of cereals, corn, soybeans, rice,millets, oilseed rape, cotton, sugarcane, potatoes, legumes, turf orpermanent crops.

The compositions according to the invention can also be used ingenetically modified plants. The term “genetically modified plants” isto be understood as plants whose genetic material has been modified bythe use of recombinant DNA techniques to include an inserted sequence ofDNA that is not native to that plant species' genome or to exhibit adeletion of DNA that was native to that species' genome, wherein themodification(s) cannot readily be obtained by cross breeding,mutagenesis or natural recombination alone. Often, a particulargenetically modified plant will be one that has obtained its geneticmodification(s) by inheritance through a natural breeding or propagationprocess from an ancestral plant whose genome was the one directlytreated by use of a recombinant DNA technique. Typically, one or moregenes have been integrated into the genetic material of a geneticallymodified plant in order to improve certain properties of the plant. Suchgenetic modifications also include but are not limited to targetedpost-translational modification of protein(s), oligo- or polypeptides,e.g., by inclusion therein of amino acid mutation(s) that permit,decrease, or promote glycosylation or polymer additions such asprenylation, acetylation farnesylation, or PEG moiety attachment.

Plants that have been modified by breeding, mutagenesis or geneticengineering, e.g. have been rendered tolerant to applications ofspecific classes of herbicides, such as auxinic herbicides such asdicamba or 2,4-D; bleacher herbicides such as 4-hydroxyphenylpyruvatedioxygenase (HPPD) inhibitors or phytoene desaturase (PDS) inhibitors;acetolactate synthase (ALS) inhibitors such as sulfonylureas orimidazolinones; enolpyruvyl shikimate 3-phosphate synthase (EPSP)inhibitors such as glyphosate; glutamine synthetase (GS) inhibitors suchas glufosinate; protoporphyrinogen-IX oxidase inhibitors (PPO); lipidbiosynthesis inhibitors such as acetylCoA carboxylase (ACCase)inhibitors; or oxynil (i.e. bromoxynil or ioxynil) herbicides as aresult of conventional methods of breeding or genetic engineering;furthermore, plants have been made resistant to multiple classes ofherbicides through multiple genetic modifications, such as resistance toboth glyphosate and glufosinate or to both glyphosate and a herbicidefrom another class such as ALS inhibitors, HPPD inhibitors, auxinicherbicides, or ACCase inhibitors. These herbicide resistancetechnologies are, for example, described in Pest Management Science 61,2005, 246; 61, 2005, 258; 61, 2005, 277; 61, 2005, 269; 61, 2005, 286;64, 2008, 326; 64, 2008, 332; Weed Science 57, 2009, 108; AustralianJournal of Agricultural Research 58, 2007, 708; Science 316, 2007, 1185;and references quoted therein. Several cultivated plants have beenrendered tolerant to herbicides by mutagenesis and conventional methodsof breeding, e.g., Clearfield® summer rape (Canola, BASF SE, Germany)being tolerant to imidazolinones, e.g., imazamox, or ExpressSun®sunflowers (DuPont, USA) being tolerant to sulfonyl ureas, e.g.,tribenuron. Genetic engineering methods have been used to rendercultivated plants such as soybean, cotton, corn, beets and rape,tolerant to herbicides such as glyphosate, imidazolinones andglufosinate, some of which are under development or commerciallyavailable under the brands or trade names RoundupReady® (glyphosatetolerant, Monsanto, USA), Cultivance® (imidazolinone tolerant, BASF SE,Germany) and LibertyLink® (glufosinate tolerant, Bayer CropScience,Germany).

Furthermore, plants are also covered that are by the use of recombinantDNA techniques capable to synthesize one or more insecticidal proteins,especially those known from the bacterial genus Bacillus, particularlyfrom Bacillus thuringiensis, such as delta-endotoxins, e.g., CryIA(b),CryIA(c), CryIF, CryIF(a2), CryIIA(b), CryIIIA, CryIIIB(b1) or Cry9c;vegetative insecticidal proteins (VIP), e.g., VIP1, VIP2, VIP3 or VIP3A;insecticidal proteins of bacteria colonizing nematodes, e.g.,Photorhabdus spp. or Xenorhabdus spp.; toxins produced by animals, suchas scorpion toxins, arachnid toxins, wasp toxins, or otherinsect-specific neurotoxins; toxins produced by fungi, such asStreptomycetes toxins, plant lectins, such as pea or barley lectins;agglutinins; proteinase inhibitors, such as trypsin inhibitors, serineprotease inhibitors, patatin, cystatin or papain inhibitors;ribosome-inactivating proteins (RIP), such as ricin, maize-RIP, abrin,luffin, saporin or bryodin; steroid metabolism enzymes, such as3-hydroxy-steroid oxidase, ecdysteroid-IDP-glycosyl-transferase,cholesterol oxidases, ecdysone inhibitors or HMG-CoA-reductase; ionchannel blockers, such as blockers of sodium or calcium channels;juvenile hormone esterase; diuretic hormone receptors (helicokininreceptors); stilbene synthase, bibenzyl synthase, chitinases orglucanases. In the context of the present invention these insecticidalproteins or toxins are to be understood expressly also as includingpre-toxins, hybrid proteins, truncated or otherwise modified proteins.Hybrid proteins are characterized by a new combination of proteindomains, (see, e.g., WO 02/015701). Further examples of such toxins orgenetically modified plants capable of synthesizing such toxins aredisclosed, e.g., in EP-A 374 753, WO 93/007278, WO 95/34656, EP-A 427529, EP-A 451 878, WO 03/18810 and WO 03/52073. The methods forproducing such genetically modified plants are generally known to theperson skilled in the art and are described, e.g., in the publicationsmentioned above. These insecticidal proteins contained in thegenetically modified plants impart to the plants producing theseproteins tolerance to harmful pests from all taxonomic groups ofarthropods, especially to beetles (Coleoptera), two-winged insects(Diptera), and moths (Lepidoptera) and to nematodes (Nematoda).Genetically modified plants capable to synthesize one or moreinsecticidal proteins are, e.g., described in the publications mentionedabove, and some of which are commercially available such as YieldGard®(corn cultivars producing the Cry1Ab toxin), YieldGard® Plus (corncultivars producing Cry1Ab and Cry3Bb1 toxins), Starlink® (corncultivars producing the Cry9c toxin), Herculex® RW (corn cultivarsproducing Cry34Ab1, Cry35Ab1 and the enzymePhosphinothricin-N-Acetyltransferase [PAT]); NuCOTN® 33B (cottoncultivars producing the Cry1Ac toxin), Bollgard® I (cotton cultivarsproducing the Cry1Ac toxin), Bollgard® II (cotton cultivars producingCry1Ac and Cry2Ab2 toxins); VIPCOT® (cotton cultivars producing aVIP-toxin); NewLeaf® (potato cultivars producing the Cry3A toxin);Bt-Xtra®, NatureGard®, KnockOut®, BiteGard®, Protecta®, Bt11 (e.g.,Agrisure® CB) and Bt176 from Syngenta Seeds SAS, France, (corn cultivarsproducing the Cry1Ab toxin and PAT enzyme), MIR604 from Syngenta SeedsSAS, France (corn cultivars producing a modified version of the Cry3Atoxin, c.f. WO 03/018810), MON 863 from Monsanto Europe S.A., Belgium(corn cultivars producing the Cry3Bb1 toxin), IPC 531 from MonsantoEurope S.A., Belgium (cotton cultivars producing a modified version ofthe Cry1Ac toxin) and 1507 from Pioneer Overseas Corporation, Belgium(corn cultivars producing the Cry1F toxin and PAT enzyme).

Furthermore, plants are also covered that are by the use of recombinantDNA techniques capable to synthesize one or more proteins to increasethe resistance or tolerance of those plants to bacterial, viral orfungal pathogens. Examples of such proteins are the so-called “pathogenesis-related proteins” (PR proteins, see, e.g., EP-A 392 225),plant disease resistance genes (e.g., potato culti-vars, which expressresistance genes acting against Phytophthora infestans derived from theMexican wild potato, Solanum bulbocastanum) or T4-lyso-zym (e.g., potatocultivars capable of synthesizing these proteins with increasedresistance against bacteria such as Erwinia amylovora). The methods forproducing such genetically modified plants are generally known to theperson skilled in the art and are described, e.g., in the publicationsmentioned above.

Furthermore, plants are also covered that are by the use of recombinantDNA techniques capable to synthesize one or more proteins to increasethe productivity (e.g., bio-mass production, grain yield, starchcontent, oil content or protein content), tolerance to drought, salinityor other growth-limiting environmental factors or tolerance to pests andfungal, bacterial or viral pathogens of those plants.

Furthermore, plants are also covered that contain by the use ofrecombinant DNA techniques a modified amount of ingredients or newingredients, specifically to improve human or animal nutrition, e.g.,oil crops that produce health-promoting long-chain omega-3 fatty acidsor unsaturated omega-9 fatty acids (e.g., Nexera® rape, DowAgroSciences, Canada).

Furthermore, plants are also covered that contain by the use ofrecombinant DNA techniques a modified amount of ingredients or newingredients, specifically to improve raw material production, e.g.,potatoes that produce increased amounts of amylopectin (e.g. Amflora®potato, BASF SE, Germany).

Furthermore, it has been found that the the compositions according tothe invention are also suitable for the defoliation and/or desiccationof plant parts, for which crop plants such as cotton, potato, oilseedrape, sunflower, soybean or field beans, in particular cotton, aresuitable. In this regard compositions have been found for thedesiccation and/or defoliation of plants, processes for preparing thesecompositions, and methods for desiccating and/or defoliating plantsusing the compositions according to the invention.

As desiccants, the compositions according to the invention are suitablein particular for desiccating the above-ground parts of crop plants suchas potato, oilseed rape, sunflower and soybean, but also cereals. Thismakes possible the fully mechanical harvesting of these important cropplants.

Also of economic interest is the facilitation of harvesting, which ismade possible by concentrating within a certain period of time thedehiscence, or reduction of adhesion to the tree, in citrus fruit,olives and other species and varieties of pomaceous fruit, stone fruitand nuts. The same mechanism, i.e. the promotion of the development ofabscission tissue between fruit part or leaf part and shoot part of theplants is also essential for the controlled defoliation of usefulplants, in particular cotton.

Moreover, a shortening of the time interval in which the individualcotton plants mature leads to an increased fiber quality afterharvesting.

USE EXAMPLES

The following examples serve to illustrate the invention.

The herbicidal action of the compositions according to the invention wasdemonstrated by the following greenhouse experiments:

The culture containers used were plastic pots containing medium loamysand with approximately 4.6% of humus and 69.9% sand as substrate. Theseeds of the test plants were sown separately for each species.

For the pre-emergence treatment, the active compounds, suspended oremulsified in water, were applied directly after sowing by means offinely distributing nozzles. The containers were irrigated gently topromote germination and growth and subsequently covered with transparentplastic hoods until the plants had rooted. This cover caused uniformgermination of the test plants unless this was adversely affected by theactive compounds.

For the post-emergence treatment, the test plants were grown to a plantheight of from 1 to 15 cm, depending on the plant habit, and only thentreated with the active compounds which had been suspended or emulsifiedin water. To this end, the test plants were either sown directly, andgrown in the same containers, or they were first grown separately asseedlings and transplanted into the test containers a few days prior totreatment.

Depending on the species, the plants were kept at 10-25° C. and 20-35°C., respectively.

The test period extended over 1 to 3 weeks. During this time, the plantswere tended and their response to the individual treatments wasevaluated 20 days after treatment except mentioned otherwise.

Evaluation was carried out using a scale from 0 to 100. 100 means noemergence of the plants, or complete destruction of at least theabove-ground parts, and 0 means no damage or normal course of growth.

The respective stated components A and B, and, if appropriate, C, wereformulated as a 10% by weight strength emulsion concentrate and, withaddition of the amount of solvent system, introduced into the sprayliquor used for applying the active compound. In the examples, thesolvent used was water.

In the examples below, using the method of S. R. Colby (1967)“Calculating synergistic and antagonistic responses of herbicidecombinations”, Weeds 15, p. 22 ff., the value E, which is expected ifthe activity of the individual active compounds is only additive, wascalculated.

E=X+Y−(X·Y/100)

where

X=percent activity using active compound A at an application rate a;

Y=percent activity using active compound B at an application rate b;

E=expected activity (in %) by A+B at application rates a+b.

If the value found experimentally is higher than the value E calculatedaccording to Colby, a synergistic effect is present.

The plants used in the greenhouse experiments were of the followingspecies:

Bayer code Scientific name ABUTH Abutilon theophrast ALOMY Alopecurusmyosuroides AMARE Amaranthus retroflexus AMBEL Ambrosia artemisiifoliaAPESV Apera spica-venti CHEAL Chenopodium album CONAR Convolvulusarvensis DIGSA Digitaria sanguinalis ECHCG Echinochloa crus-galli ERICAConyza canadensis GALAP Galium aparine GERDI Geranium dissectum GERPUGeranium pusillum IPOHE Ipomoea hederacea KCHSC Kochia scoparia LAMAMLamium amplexicaule LOLMU Lolium multiflorum MATCH Matricaria recutitaPANMI Panicum miliaceum PAPRH Papaver rhoeas POLAV Polygonum avicularePOLCO Polygonum convolvulus POLPE Persicaria maculosa SASKR Salsola kaliSEBEX Sesbania exaltata SETVI Setaria viridis STEME Stellaria mediaVIOAR Viola arvensis note: 100-90%: “very good” 90-80%: “good”

The results of these tests are given below in the use examples anddemonstrate the synergistic effect of the mixtures comprising at leastone compound of the formula (I) and at least one herbicide B. In thiscontext, a.i. means active ingredient, based on 100% active ingredient.

Use Example 1

Synergistic herbicidal action of the composition 1.190 applied by thepost emergence method: treatment by the mixture of compound(I.1)+chlorotoluron (B.190)

application rate herbicidal activity against a.i. in g/ha POLCO AMARESTEME GERDI IPOHE I.1 B.190 found calculated found calculated foundcalculated found calculated found calculated 31.25 — 50 — 35 — 70 — 30 —65 — — 62.5 50 — 40 — 70 — 60 — 60 — 31.25 62.5 100 75 98 61 100 91 10072 100 86 application rate herbicidal activity against a.i. in g/haPOLCO IPOHE POLAV AMARE CHEAL I.1 B.190 found calculated foundcalculated found calculated found calculated found calculated 15.6 — 30— 50 — 45 — 30 — 70 — — 62.5 50 — 60 — 50 — 40 — 95 — 15.6 62.5 100 65100 80 100 73 98 58 100 99

Use Example 2

Synergistic herbicidal action applied by the post emergence method:treatment by the mixture of compound (I.1)+bentazon in form ofsodium-salt (bentazon Na)

application rate herbicidal activity against a.i. in g/ha POLCO AMAREPOLAV I.1 bentazon Na found calculated found calculated found calculated31.25 — 50 — 35 — 80 — — 125 40 — 75 — 40 — 31.25 125 90 70 98 84 90 88

Use Example 3

Synergistic herbicidal action of the composition 1.67 applied by thepost emergence method: treatment by the mixture of compound(I.1)+atrazine (B.67)

application rate herbicidal activity against a.i. in g/ha LOLMU PHACAGERDI MATCH CONAR I.1 B.67 found calculated found calculated foundcalculated found calculated found calculated 62.5 — 20 — 35 — 40 — 0 — 0— — 125 35 — 30 — 70 — 50 — 65 — 62.5 125 80 48 70 55 100 82 100 50 9865 application rate herbicidal activity against a.i. in g/ha ABUTH I.1B.67 found calculated found calculated found calculated found calculatedfound calculated 62.5 — 90 — — — — — — 125 60 — — — — — 62.5 125 100 96application rate a.i. in herbicidal activity against g/ha ABUTH STEMEMATCH GERDI I.1 B.67 found calculated found calculated found calculatedfound calculated 31.25 — 60 — 70 — 30 — 30 — — 125 60 — 75 — 70 — 85 —31.25 125 95 84 100 93 100 79 100 90 application rate herbicidalactivity against a.i. in g/ha LOLMU PHACA POLCO CHEAL GALAP I.1 B.67found calculated found calculated found calculated found calculatedfound calculated 31.25 — 0 — 0 — 0 — 65 — 75 — — 125 35 — 30 — 60 — 80 —70 — 31.25 125 80 35 70 0 100 60 98 93 100 93 application rateherbicidal activity against a.i. in g/ha ABUTH MATCH CONAR STEME GERDII.1 B.67 found calculated found calculated found calculated foundcalculated found calculated 31.25 — 60 — 30 — 0 — 70 — 30 — — 125 60 —70 — 65 — 75 — 85 — 31.25 125 95 84 100 79 95 65 100 93 100 90application rate herbicidal activity against a.i. in g/ha CHEAL GERDIPOLCO GALAP I.1 B.67 found calculated found calculated found calculatedfound calculated found calculated 15.6 — 0 — 0 — 0 — 20 — — — 125 80 —70 — 60 — 70 — — 15.6 125 98 80 100 70 70 60 85 76 application rateherbicidal activity against a.i. in g/ha LOLMU ABUTH STEME CONAR I.1B.67 found calculated found calculated found calculated found calculatedfound calculated 15.6 — 0 — 30 — 0 — 0 — — — 125 35 — 60 — 75 — 65 — —15.6 125 70 35 85 72 100 75 98 65 application rate herbicidal activityagainst a.i. in g/ha GERDI LOLMU ABUTH CONAR I.1 B.67 found calculatedfound calculated found calculated found calculated found calculated 7.8— 0 — 0 — 0 — 0 — — — 125 70 — 35 — 60 — 65 — — 7.8 125 100 70 60 35 8060 98 65 application rate herbicidal activity against a.i. in g/ha ALOMYLOLMU ECHCG GALAP CONAR I.1 B.67 found calculated found calculated foundcalculated found calculated found calculated 62.5 — 0 — 40 — 65 — 10 —25 — — 62.5 35 — 20 — 35 — 65 — 60 — 62.5 62.5 65 35 65 52 85 77 90 6985 70 application rate herbicidal activity against a.i. in g/ha POLCOI.1 B.67 found calculated found calculated found calculated foundcalculated found calculated 62.5 — 65 — — — — — — 62.5 80 — — — — — 62.562.5 100 93 application rate herbicidal activity against a.i. in g/haALOMY POLCO CHEAL GALAP STEME I.1 B.67 found calculated found calculatedfound calculated found calculated found calculated 20.8 — 0 — 30 — 85 —0 — 50 — — 62.5 35 — 80 — 75 — 65 — 80 — 20.8 62.5 50 35 100 86 100 9670 65 100 90 application rate herbicidal activity against a.i. in g/haCONAR ECHCG I.1 B.67 found calculated found calculated found calculatedfound calculated found calculated 20.8 — 0 — 30 — — — — — 62.5 60 — 35 —— — — 20.8 62.5 65 60 60 55 application rate herbicidal activity againsta.i. in g/ha ALOMY STEME APESV CHEAL I.1 B.67 found calculated foundcalculated found calculated found calculated found calculated 6.9 — 0 —0 — 0 — 0 — — — 62.5 35 — 80 — 60 — 75 — — 6.9 62.5 40 35 100 80 65 6085 75 application rate herbicidal activity against a.i. in g/ha STEMEAPESV I.1 B.67 found calculated found calculated found calculated foundcalculated found calculated 2.3 — 0 — 0 — — — — — 62.5 80 — 60 — — — —2.3 62.5 100 80 65 60

Use Example 4

Synergistic herbicidal action of the composition 1.69 applied by thepost emergence method: treatment by the mixture of compound(I.1)+bromoxynil (B.69)

application rate herbicidal activity against a.i. in g/ha ABUTH CHEALGALAP ERICA CONAR I.1 B.69 found calculated found calculated foundcalculated found calculated found calculated 62.5 — 50 — 60 — 65 — 90 —65 — — 25 35 — 60 — 50 — 30 — 50 — 62.5 25 85 68 100 84 100 83 100 93100 83 application rate herbicidal activity against a.i. in g/ha CHEALCONAR MATCH I.1 B.69 found calculated found calculated found calculated31.25 — 30 — 70 — 30 — — 25 60 — 50 — 0 — 31.25 25 85 72 100 85 100 30

Use Example 5

Synergistic herbicidal action of the composition 1.191 applied by thepost emergence method: treatment by the mixture of compound(I.1)+pyridate (B.191)

application rate herbicidal activity against a.i. in g/ha GALAP STEMEMATCH ERICA I.1 B.191 found calculated found calculated found calculatedfound calculated 62.5 — 65 — 85 — 30 — 90 — — 225 90 — 0 — 20 — 70 —62.5 225 100 97 100 85 95 44 100 97

Use Example 6

Synergistic herbicidal action of the composition 1.76 applied by thepost emergence method: treatment by the mixture of compound(I.1)+isoproturon (B.76)

application rate herbicidal activity against a.i. in g/ha CHEAL CONARDIGSA I.1 B.76 found calculated found calculated found calculated 62.5 —60 — 65 — 40 — — 225 65 — 65 — 30 — 62.5 225 100 86 100 88 65 58application rate herbicidal activity against a.i. in g/ha AMARE CHEALDIGSA I.1 B.76 found calculated found calculated found calculated 31.25— 90 — 30 — 35 — — 225 50 — 65 — 30 — 31.25 225 98 95 100 76 60 55

Use Example 7

Synergistic herbicidal action of the composition 1.82 applied by thepost emergence method: treatment by the mixture of compound(I.1)+terbuthylazine (B.82)

application rate herbicidal activity against a.i. in g/ha CHEAL GALAPI.1 B.82 found calculated found calculated 62.5 — 60 — 65 — — 31.25 65 —55 — 62.5 31.25 100 86 85 84

Use Example 8

Synergistic herbicidal action of the composition 1.77 applied by thepost emergence method: treatment by the mixture of compound(I.1)+linuron (B.77)

application rate herbicidal activity against a.i. in g/ha LOLMU GALAPCONAR I.1 B.77 found calculated found calculated found calculated 62.5 —20 — 10 — 25 — — 75 35 — 40 — 50 — 62.5 75 60 48 65 46 85 63

Use Example 9

Synergistic herbicidal action of the composition 1.79 applied by thepost emergence method: treatment by the mixture of compound(I.1)+metribuzin (B.79)

application rate herbicidal activity against a.i. in g/ha ECHCG POLCOI.1 B.79 found calculated found calculated 62.5 — 65 — 75 — — 25 20 — 20— 62.5 25 75 72 100 80 application rate herbicidal activity against a.i.in g/ha POLCO MATCH I.1 B.79 found calculated found calculated 20.8 — 50— 60 — — 25 20 — 65 — 20.8 25 90 60 98 86

Use Example 10

Synergistic herbicidal action of the composition 1.192 applied by thepost emergence method: treatment by the mixture of compound(I.1)+phenmedipham (B.192)

application rate herbicidal activity against a.i. in g/ha SETVI AMARECHEAL MATCH AMBEL I.1 B.192 found calculated found calculated foundcalculated found calculated found calculated 20.8 — 25 — 70 — 85 — 60 —30 — — 62.5 65 — 35 — 50 — 50 — 90 — 20.8 62.5 75 74 95 81 95 93 100 8098 93

Use Example 11

Synergistic herbicidal action of the composition 1.80 applied by thepost emergence method: treatment by the mixture of compound(I.1)+propanil (B.80)

application rate herbicidal activity against a.i. in g/ha DIGSA CONARERICA I.1 B.80 found calculated found calculated found calculated 62.5 —40 — 25 — 65 — — 250 40 — 20 — 65 — 62.5 250 65 64 70 40 98 88

Use Example 12

Synergistic herbicidal action of the composition 1.107 applied by thepost emergence method: treatment by the mixture of compound(I.1)+topramezone (B.107)

application rate herbicidal activity against a.i. in g/ha POLCO ABUTHGALAP ERICA I.1 B.107 found calculated found calculated found calculatedfound calculated 62.5 — 75 — 65 — 10 — 65 — — 6 35 — 85 — 70 — 65 — 62.56 100 54 95 95 80 73 98 88 application rate herbicidal activity againsta.i. in g/ha MATCH ERICA ABUTH I.1 B.107 found calculated foundcalculated found calculated 20.8 — 60 — 65 — 0 — — 6 70 — 65 — 85 — 20.86 95 88 100 88 90 85

Use Example 13

Synergistic herbicidal action of the composition 1.113 applied by thepost emergence method: treatment by the mixture of compound(I.1)+glyphosate (B.113)

application rate herbicidal activity against a.i. in g/ha PANMI GALAPGERDI I.1 B.113 found calculated found calculated found calculated 125 —60 — 80 — 80 — — 135 90 — 80 — 80 — 125 135 98 96 98 96 98 96application rate herbicidal activity against a.i. in g/ha PANMI GALAPCONAR I.1 B.113 found calculated found calculated found calculated 125 —60 — 80 — 80 — — 33.75 80 — 50 — 45 — 125 33.75 95 92 98 90 100 89

Use Example 14

Synergistic herbicidal action of the composition 1.193 applied by thepost emergence method: treatment by the mixture of compound(I.1)+(1RS,2SR,4SR)-1,4-epoxy-p-menth-2-yl2-methylbenzyl ether (B.193)

application rate herbicidal activity against a.i. in g/ha ECHCG DIGSAGERDI ALOMY I.1 B.193 found calculated found calculated found calculatedfound calculated 250 — 95 — 35 — 95 — 45 — — 15 40 — 20 — 40 — 0 — 25015 98 97 80 48 98 97 60 45

Use Example 15

Synergistic herbicidal action of the composition 1.030 applied by thepost emergence method: treatment by the mixture of compound(I.1)+imazamox (B.30)

application rate herbicidal activity against a.i. in g/ha VIOAR CONARGERDI I.1 B.30 found calculated found calculated found calculated 62.5 —0 — 25 — 85 — — 3.75 45 — 85 — 90 — 62.5 3.75 65 45 90 89 100 99

Use Example 16

Synergistic herbicidal action of the composition 1.84 applied by thepost emergence method: treatment by the mixture of compound(I.1)+paraquat-dichloride (B.84)

application rate herbicidal activity against a.i. in g/ha AMBEL VIOARSASKR ERICA GALAP I.1 B.84 found calculated found calculated foundcalculated found calculated found calculated 31.25 — 65 — 40 — 10 — 55 —65 — — 17.5 90 — 55 — 70 — 35 — 55 — 31.25 17.5 100 97 75 73 98 73 75 7185 84 application rate herbicidal activity against a.i. in g/ha MATCHVIOAR POLCO CONAR I.1 B.84 found calculated found calculated foundcalculated found calculated 62.5 — 80 — 40 — 90 — 45 — — 17.5 80 — 55 —30 — 10 — 62.5 17.5 98 96 75 73 95 93 60 51

Use Example 17

Synergistic herbicidal action of the composition 1.87 applied by thepost emergence method: treatment by the mixture of compound(I.1)+carfentrazone-ethyl (B.87)

application rate a.i. in herbicidal activity against g/ha LAMAM PAPRHMATCH GERDI I.1 B.87 found calculated found calculated found calculatedfound calculated 62.5 — 85 — 85 — 80 — 85 — — 1.75 80 — 30 — 75 — 70 —62.5 1.75 100 97 100 90 98 95 98 96 application rate a.i. in herbicidalactivity against g/ha LALAM SEBEX MATCH GERPU I.1 B.87 found calculatedfound calculated found calculated found calculated 31.25 — 70 — 75 — 35— 80 — — 1.75 80 — 75 — 75 — 75 — 31.25 1.75 98 94 100 94 95 84 98 95

Use Example 18

Synergistic herbicidal action of the composition 1.139 applied by thepost emergence method: treatment by the mixture of compound(I.1)+pyroxasulfone (B.139)

application rate a.i. in herbicidal activity against g/ha GERPU LAMAMSEBEX CONAR ABUTH I.1 B.139 found calculated found calculated foundcalculated found calculated found calculated 31.25 — 80 — 80 — 80 — 30 —10 — — 25 25 — 45 — 35 — 60 — 60 — 31.25 25 98 85 90 89 95 87 75 72 7564 application rate a.i. in herbicidal activity against g/ha GERPU AMBELCONAR POLCO POLPE I.1 B.139 found calculated found calculated foundcalculated found calculated found calculated 31.25 — 80 — 65 — 30 — 65 —30 — — 12.5 0 — 10 — 60 — 15 — 55 — 31.25 12.5 95 80 75 69 80 72 80 7080 69

Use Example 19

Synergistic herbicidal action of the composition 1.92 applied by thepost emergence method: treatment by the mixture of compound(I.1)+saflufenacil (B.92)

application rate herbicidal activity against a.i. in g/ha ERICA GALAPI.1 B.92 found calculated found calculated 31.25 — 25 — 65 — — 0.5 80 —80 — 31.25 0.5 100 85 98 93

Use Example 20

Synergistic herbicidal action of the composition 1.100 applied by thepost emergence method: treatment by the mixture of compound(I.1)+isoxaflutole (B.100)

application rate a.i. in herbicidal activity against g/ha VIOAR AMBELERICA GERDI I.1 B.100 found calculated found calculated found calculatedfound calculated 62.5 — 30 — 90 — 75 — 65 — — 12.5 70 — 45 — 80 — 0 —62.5 12.5 85 79 98 95 100 95 100 65 application rate a.i. in herbicidalactivity against g/ha POLCO AMBEL ERICA GERDI I.1 B.100 found calculatedfound calculated found calculated found calculated 31.25 — 70 — 90 — 25— 60 — — 12.5 60 — 45 — 80 — 0 — 31.25 12.5 95 88 98 95 98 85 90 60

Use Example 21

Synergistic herbicidal action of the composition 1.40 applied by thepost emergence method: treatment by the mixture of compound(I.1)+imazethapyr (B.40)

application rate a.i. in herbicidal activity against g/ha PAPRH IPOHEGERDI I.1 B.40 found calculated found calculated found calculated 62.5 —65 — 95 — 70 — — 7.5 45 — 80 — 90 — 62.5 7.5 100 81 100 99 98 97application rate a.i. in herbicidal activity against g/ha ECHCG POLCOGERDI I.1 B.40 found calculated found calculated found calculated 31.25— 0 — 20 — 30 — — 7.5 85 — 80 — 95 — 31.25 7.5 90 85 90 84 98 97

Use Example 22

Synergistic herbicidal action of the composition 1.104 applied by thepost emergence method: treatment by the mixture of compound(I.1)+sulcotrione (B.104)

application rate a.i. in herbicidal activity against g/ha ECHCG VIOARMATCH I.1 B.104 found calculated found calculated found calculated 31.25— 0 — 0 — 10 — — 15 80 — 85 — 10 — 31.25 15 98 80 100 85 100 19application rate a.i. in herbicidal activity against g/ha ERICA POLCOGERDI KCHSC I.1 B.104 found calculated found calculated found calculatedfound calculated 31.25 — 25 — 70 — 30 — 75 — — 15 75 — 90 — 45 — 90 —31.25 15 95 81 98 97 75 62 100 98

Use Example 23

Synergistic herbicidal action of the composition 1.2605 applied by thepost emergence method: treatment by the mixture of compound(I.1)+fenoxaprop-ethyl (B.5)+mefenpyr-diethyl (C.13)

herbicidal activity against application rate APESV GALAP a.i. in g/hacal- POLCO cal- I.1 B.5 C.13 found culated found calculated foundculated 31.25 — — 0 — 45 — 50 — — 7.5 8.15 65 — 0 — 0 — 31.25 7.5 8.1575 65 60 45 60 50

Use Example 24

Synergistic herbicidal action of the composition 1.59 applied by thepost emergence method: treatment by the mixture of compound(I.1)+rimsulfuron (B.59)

application rate a.i. in herbicidal activity against g/ha PAPRH ERICAIPOHE I.1 B.59 found calculated found calculated found calculated 31.25— 50 — 25 — 75 — — 0.5 65 — 65 — 90 — 31.25 0.5 85 83 75 74 98 98application rate herbicidal activity against a.i. in g/ha MATCH GERDII.1 B.59 found calculated found calculated 62.5 — 50 — 90 — — 0.5 75 —75 — 62.5 0.5 100 88 100 98

Use Example 25

Synergistic herbicidal action of the composition 1.120 applied by thepost emergence method: treatment by the mixture of compound(I.1)+glufosinate ammonium (B.120)

application rate a.i. in herbicidal activity against g/ha VIOAR POLCOABUTH GERDI GALAP I.1 B.120 found calculated found calculated foundcalculated found calculated found calculated 31.25 — 0 — 25 — 25 — 40 —50 — — 125 15 — 65 — 70 — 90 — 80 — 31.25 125 80 15 95 74 90 78 98 94 9890 application rate a.i. in herbicidal activity against g/ha PAPRH MATCHIPOHE GERDI KCHSC I.1 B.120 found calculated found calculated foundcalculated found calculated found calculated 31.25 — 50 — 0 — 75 — 35 —90 — — 62.5 30 — 55 — 80 — 40 — 45 — 31.25 62.5 85 65 95 55 98 95 95 61100 95

Use Example 26

Synergistic herbicidal action of the composition 1.02 applied by thepost emergence method: treatment by the mixture of compound(I.1)+clodinafop-propargyl (B.2)

application rate a.i. in herbicidal activity against g/ha ALOMY MATCHIPOHE ABUTH I.1 B.2 found calculated found calculated found calculatedfound calculated 62.5 — 20 — 70 — 90 — 25 — — 15 85 — 0 — 40 — 15 — 62.515 90 88 80 70 98 94 75 36 application rate a.i. in herbicidal activityagainst g/ha GERDI STEME POHE GALAP I.1 B.2 found calculated foundcalculated found calculated found calculated 62.5 — 90 — 65 — 90 — 50 —— 7.5 0 — 0 — 10 — 0 — 62.5 7.5 98 90 80 65 98 91 65 50

Use Example 27

Synergistic herbicidal action of the composition 1.44 applied by thepost emergence method: treatment by the mixture of compound(I.1)+iodosulfuron methyl sodium (B.44)

application rate a.i. in herbicidal activity against g/ha ALOMY POLCOI.1 B.44 found calculated found calculated 62.5 — 0 — 40 — — 1 20 — 90 —62.5 1 55 20 98 94

Use Example 28

Synergistic herbicidal action of the composition 1.60 applied by thepost emergence method: treatment by the mixture of compound(I.1)+sulfosulfuron (B.60)

application rate a.i. in herbicidal activity against g/ha ALOMY APESVPOLCO PAPRH I.1 B.60 found calculated found calculated found calculatedfound calculated 62.5 — 0 — 0 — 40 — 50 — — 3 60 — 60 — 90 — 90 — 62.5 385 60 85 60 98 94 100 95 application rate herbicidal activity againsta.i. in g/ha VIOAR ERICA POLCO I.1 B.60 found calculated foundcalculated found calculated 31.25 — 20 — 0 — 30 — — 3 65 — 75 — 90 —31.25 3 85 72 80 75 95 93

Use Example 29

Synergistic herbicidal action of the composition 1.26 applied by thepost emergence method: treatment by the mixture of compound(I.1)+florasulam (B.26)

application rate a.i. in herbicidal activity against g/ha POLCO PAPRHI.1 B.26 found calculated found calculated 31.25 — 70 — 50 — — 2 85 — 98— 31.25 2 98 96 100 99

Use Example 30

Synergistic herbicidal action of the composition 1.35 applied by thepost emergence method: treatment by the mixture of compound(I.1)+imazapyr (B.35)

application rate a.i. in herbicidal activity against g/ha ABUTH GERDIMATCH I.1 B.35 found calculated found calculated found calculated 31.25— 10 — 30 — 40 — — 10 90 — 95 — 55 — 31.25 10 95 91 98 97 98 73application rate a.i. in herbicidal activity against g/ha POLCO VIOARERICA I.1 B.35 found calculated found calculated found calculated 31.25— 30 — 25 — 0 — — 5 95 — 55 — 75 — 31.25 5 98 97 70 66 80 75

Use Example 31

Synergistic herbicidal action of the composition 1.101 applied by thepost emergence method: treatment by the mixture of compound(I.1)+mesotrione (B.101)

application herbicidal activity against rate a.i. in PAPRH g/ha cal-AMBEL SASKR I.1 B.101 found culated found calculated found calculated31.25 — 0 — 85 — 20 — — 9.375 35 — 80 — 75 — 31.25 9375 75 35 100 97 10080 application herbicidal activity against rate a.i. in MATCH g/ha cal-ERICA GERDI I.1 B.101 found culated found calculated found calculated31.25 — 35 — 35 — 55 — — 9.375 75 — 80 — 0 — 31.25 9375 100 84 95 87 8055

Use Example 32

Synergistic herbicidal action of the composition 1.106 applied by thepost emergence method: treatment by the mixture of compound(I.1)+tembotrione (B.106)

application rate a.i. in herbicidal activity against g/ha SASKR MATCHERICA IPOHE I.1 B.106 found calculated found calculated found calculatedfound calculated 31.25 — 20 — 35 — 35 — 70 — — 9.375 65 — 65 — 90 — 70 —31.25 9375 80 72 100 77 95 94 95 91

Use Example 33

Synergistic herbicidal action of the composition 1.51 applied by thepost emergence method: treatment by the mixture of compound(I.1)+nicosulfuron (B.51)

application rate a.i. in herbicidal activity against g/ha AMBEL MATCHPOLPE I.1 B.51 found calculated found calculated found calculated 31.25— 85 — 35 — 45 — — 20 80 — 90 — 95 — 31.25 20 100 97 95 94 98 97

Use Example 34

Synergistic herbicidal action of the composition 1.164 applied by thepost emergence method: treatment by the mixture of compound (I.1)+MCPA(B.164)

application rate herbicidal activity against a.i. in g/ha GALAP POLAVCONAR I.1 B.164 found calculated found calculated found calculated foundcalculated 125 — 80 — 65 — 70 — — — 400 30 — 85 — 90 — — 125 400 95 8698 95 100 97 application rate herbicidal activity against a.i. in g/haPOLAV CONAR I.1 B. 164 found calculated found calculated foundcalculated found calculated found calculated 125 — 65 — 70 — — — — — 20085 — 90 — — — — 125 200 100 95 100 97 application rate herbicidalactivity against a.i. in g/ha VIOAR POLAV CONAR POLCO I.1 B.164 foundcalculated found calculated found calculated found calculated 62.5 — 0 —65 — 60 — 85 — — 400 70 — 85 — 90 — 50 — 62.25 400 100 70 100 95 100 96100 93 application rate herbicidal activity against a.i. in g/ha VIOARPOLAV CONAR POLCO I.1 B.164 found calculated found calculated foundcalculated found calculated 62.5 — 0 — 65 — 60 — 85 — — 200 65 — 85 — 90— 50 — 62.5 200 70 65 100 95 100 96 100 93 application rate herbicidalactivity against a.i. in g/ha VIOAR POLAV I.1 B.164 found calculatedfound calculated 62.5 — 0 — 65 — — 100 60 — 70 — 62.5 100 75 60 100 90application rate herbicidal activity against a.i. in g/ha POLPE LAMAMMATCH CONAR STEME I.1 B.164 found calculated found calculated foundcalculated found calculated found calculated 31.25 — 70 — 70 — 0 — 40 —70 — — 400 80 — 70 — 50 — 90 — 80 — 31.25 400 100 94 95 91 55 50 98 94100 94 application rate herbicidal activity against a.i. in g/ha POLPEPAPRH ABUTH STEME LAMAM I.1 B.164 found calculated found calculatedfound calculated found calculated found calculated 31.25 — 70 — 65 — 40— 70 — 70 — — 200 65 — 65 — 80 — 60 — 65 — 31.25 200 100 90 95 88 98 8895 88 95 90 application rate herbicidal activity against a.i. in g/haPAPRH GERDI STEME I.1 B.164 found calculated found calculated foundcalculated found calculated found calculated 31.25 — 65 — 70 — 70 — — —— 100 60 — 65 — 50 — — — 31.25 100 100 86 98 90 100 85

Use Example 35

Synergistic herbicidal action applied by the post emergence method:treatment by the mixture of compound (I.1)+pyrasulfatole

application rate herbicidal activity against a.i. in g/ha VIOAR CONARI.1 pyrasulfatole found calculated found calculated found calculatedfound calculated 125 — 90 — 70 — — — — 40 60 — 85 — — — 125 40 100 96 9896 application rate herbicidal activity against a.i. in g/ha CONAR I.1pyrasulfatole found calculated found calculated found calculated foundcalculated found calculated 125 — 70 — — — — — — 20 65 — — — — — 125 2098 90 application rate herbicidal activity against a.i. in g/ha VIOARCONAR I.1 pyrasulfatole found calculated found calculated foundcalculated found calculated found calculated 125 — 90 — 70 — — — — — 100 — 60 — — — — 125 10 100 90 98 88 application rate herbicidal activityagainst a.i. in g/ha VIOAR I.1 pyrasulfatole found calculated foundcalculated found calculated found calculated found calculated 62.5 — 0 —— — — — — 40 60 — — — — — 62.5 40 80 60 application rate herbicidalactivity against a.i. in g/ha VIOAR POLAV CONAR I.1 pyrasulfatole foundcalculated found calculated found calculated found calculated foundcalculated 62.5 — 0 — 65 — 60 — — — — 20 40 — 70 — 65 — — — 62.5 20 7040 100 90 90 86 application rate herbicidal activity against a.i. ing/ha VIOAR I.1 pyrasulfatole found calculated found calculated foundcalculated found calculated found calculated 62.5 — 0 — — — — — — 10 0 —— — — — 62.5 10 60 0 application rate herbicidal activity against a.i.in g/ha PAPRH MATCH CONAR GERDI VIOAR I.1 pyrasulfatole found calculatedfound calculated found calculated found calculated found calculated31.25 — 65 — 0 — 40 — 70 — 0 — — 40 65 — 50 — 85 — 50 — 60 — 31.25 40100 88 100 50 100 91 100 85 65 60 application rate herbicidal activityagainst a.i. in g/ha PAPRH VIOAR I.1 pyrasulfatole found calculatedfound calculated found calculated found calculated found calculated31.25 — 65 — 0 — — — — — 20 65 — 40 — — — — 31.25 20 100 88 50 40application rate herbicidal activity against a.i. in g/ha PAPRH VIOARMATCH CONAR SASKAR I.1 pyrasulfatole found calculated found calculatedfound calculated found calculated found calculated 31.25 — 65 — 0 — 0 —40 — 60 — — 10 50 — 0 — 50 — 60 — 90 — 31.25 10 100 83 60 0 100 50 98 76100 96

Use Example 36

Synergistic herbicidal action applied by the post emergence method:treatment by the mixture of compound (I.1)+naptalam

application rate herbicidal activity 6 days after treatment against a.i.in g/ha SORVU VIOAR POLAV SASKR I.1 naptalam found calculated foundcalculated found calculated found calculated 62.5 — 20 — 0 — 70 — 65 — —200 50 — 70 — 75 — 80 — 62.5 200 65 60 80 70 98 93 98 93 applicationrate herbicidal activity 6 days after treatment against a.i. in g/haCONAR VIOAR POLAV SASKR KCHAS I.1 naptalam found calculated foundcalculated found calculated found calculated found calculated 31.25 — 5— 0 — 70 — 65 — 10 — — 200 80 — 70 — 75 — 80 — 85 — 31.25 200 95 81 7570 98 93 98 93 95 87 application rate herbicidal activity 6 days aftertreatment against a.i. in g/ha CONAR I.1 naptalam found calculated foundcalculated found calculated found calculated found calculated 125 — 70 —— — — — — 100 80 — — — — — 125 100 98 94 application rate herbicidalactivity 6 days after treatment against a.i. in g/ha VIOAR POLAV I.1naptalam found calculated found calculated found calculated foundcalculated 62.5 — 0 — 70 — — — — 100 65 — 75 — — — 62.5 100 70 65 98 93application rate herbicidal activity 6 days after treatment against a.i.in g/ha CONAR MATCH ABUTH KCHSC I.1 naptalam found calculated foundcalculated found calculated found calculated 31.25 — 5 — 0 — 35 — 10 — —100 80 — 65 — 85 — 85 — 31.25 100 95 81 70 65 95 90 95 87 applicationrate herbicidal activity 6 days after treatment against a.i. in g/haERICA I.1 naptalam found calculated found calculated found calculatedfound calculated 125 — 70 — — — — — 50 80 — — — — 125 50 98 94application rate herbicidal activity 6 days after treatment against a.i.in g/ha MATCH POLAV SASKR POLCO I.1 naptalam found calculated foundcalculated found calculated found calculated 62.5 — 10 — 70 — 65 — 70 —— 50 30 — 70 — 70 — 75 — 62.5 50 70 37 95 91 95 90 98 93 applicationrate herbicidal activity 6 days after treatment against a.i. in g/haPOLAV MATCH CONAR POLCO I.1 naptalam found calculated found calculatedfound calculated found calculated 31.25 — 70 — 0 — 5 — 35 — — 50 70 — 30— 80 — 75 — 31.25 50 98 91 70 30 95 81 90 84

Use Example 37

Synergistic herbicidal action of the composition 1.96 applied by thepost emergence method: treatment by the mixture of compound(I.1)+benzobicyclon (B.96)

application rate herbicidal activity 6 days after treatment against a.i.in g/ha VIOAR SASKR CONAR I.1 B.96 found calculated found calculatedfound calculated found calculated 62.5 — 0 — 65 — 65 — — — 140 65 — 65 —75 — — 62.5 140 80 65 95 88 98 91 application rate herbicidal activity 6days after treatment against a.i. in g/ha POLAV IPOHE POLCO GALAP I.1B.96 found calculated found calculated found calculated found calculatedfound calculated 62.5 — 70 — 80 — 70 — 65 — — — 140 70 — 70 — 80 — 80 —— 62.5 140 95 91 98 94 98 94 98 93 application rate herbicidal activity6 days after treatment against a.i. in g/ha POLCO KCHSC VIOAR IPOHESORVU I.1 B.96 found calculated found calculated found calculated foundcalculated found calculated 31.25 — 35 — 10 — 0 — 70 — 0 — — 140 80 — 55— 65 — 70 — 60 — 31.25 140 95 87 70 60 70 65 95 91 65 60 applicationrate herbicidal activity 6 days after treatment against a.i. in g/haVIOAR POLAV POLCO GALAP KCHSC I.1 B.96 found calculated found calculatedfound calculated found calculated found calculated 62.5 — 0 — 70 — 70 —65 — 90 — — 70 65 — 70 — 70 — 75 — 40 — 62.5 70 80 65 95 91 95 91 95 9198 94 application rate herbicidal activity 6 days after treatmentagainst a.i. in g/ha POLCO KCHSC VIOAR IPOHE ABUTH I.1 B.96 foundcalculated found calculated found calculated found calculated foundcalculated 31.25 — 35 — 10 — 0 — 70 — 35 — — 70 70 — 40 — 65 — 70 — 85 —31.25 70 90 81 85 46 70 65 95 91 95 90 application rate herbicidalactivity 6 days after treatment against a.i. in g/ha VIOAR KCHSC I.1B.96 found calculated found calculated found calculated found calculatedfound calculated 62.5 — 0 — 90 — — — — — 35 65 — 35 — — — — 62.5 35 8065 98 94 application rate herbicidal activity 6 days after treatmentagainst a.i. in g/ha POLPE KCHSC ABUTH I.1 B.96 found calculated foundcalculated found calculated found calculated found calculated 31.25 — 10— 10 — 35 — — — — 35 85 — 35 — 80 — — — 31.25 35 98 87 85 42 95 87application rate herbicidal activity 6 days after treatment against a.i.in g/ha VIOAR IPOHE STEME I.1 B.96 found calculated found calculatedfound calculated found calculated found calculated 31.25 — 0 — 70 — 60 —— — — 35 65 — 70 — 85 — — — 31.25 35 70 65 95 91 98 94

Use Example 38

Synergistic herbicidal action of the composition 1.20 applied by thepost emergence method: treatment by the mixture of compound(I.1)+bispyribac-sodium (B.20)

application rate herbicidal activity against a.i. in g/ha ALOMY I.1 B.20Found calculated found calculated found calculated found calculated 125— 30 — — — — — 4 55 — — — — 125 4 80 69 application rate herbicidalactivity against a.i. in g/ha ALOMY APESV I.1 B.20 found calculatedfound calculated found calculated found calculated found calculated 62.5— 25 — 20 — — — — — 4 55 — 60 — — — — 62.5 4 70 66 75 68 applicationrate herbicidal activity against a.i. in g/ha ABUTH I.1 B.20 foundcalculated found calculated found calculated found calculated foundcalculated 31.25 — 15 — — — — — — 4 65 — — — — — 31.25 4 90 70application rate herbicidal activity against a.i. in g/ha ALOMY I.1 B.20found calculated found calculated found calculated found calculatedfound calculated 125 — 30 — — — — — — 2 30 — — — — — 125 2 60 51application rate herbicidal activity against a.i. in g/ha ABUTH IPOHEI.1 B.20 found calculated found calculated found calculated foundcalculated found calculated 31.25 — 15 — 25 — — — — — 2 35 — 30 — — — —31.25 2 60 45 60 48

Use Example 39

Synergistic herbicidal action of the composition 1.24 applied by thepost emergence method: treatment by the mixture of compound(I.1)+cyclosulfamuron (B.24)

application rate herbicidal activity against a.i. in g/ha MATCH ALOMYI.1 B.24 found calculated found calculated found calculated foundcalculated 125 — 75 — 30 — — — — 2 65 — 35 — — — 125 2 100 91 60 55application rate herbicidal activity against a.i. in g/ha MATCH KCHSCABUTH I.1 B.24 found calculated found calculated found calculated foundcalculated found calculated 31.25 — 25 — 40 — 15 — — — — 2 65 — 45 — 85— — — 31.25 2 85 74 80 67 90 87 application rate herbicidal activityagainst a.i. in g/ha ALOMY I.1 B.24 found calculated found calculatedfound calculated found calculated found calculated 125 — 30 — — — — — —1 25 — — — — — 125 1 55 48 application rate herbicidal activity againsta.i. in g/ha IPOHE KCHSC APESV I.1 B.24 found calculated foundcalculated found calculated found calculated found calculated 31.25 — 25— 40 — 20 — — — — 1 75 — 45 — 0 — — — 31.25 1 95 81 75 67 30 20

Use Example 40

Synergistic herbicidal action of the composition 1.63 applied by thepost emergence method: treatment by the mixture of compound(I.1)+tribenuron-methyl (B.63)

application rate herbicidal activity against a.i. in g/ha POLCO VIOARI.1 B.63 found calculated found calculated found calculated foundcalculated 125 — 80 — 0 — — — — 1 30 — 40 — — — 125 1 100 86 98 40application rate herbicidal activity against a.i. in g/ha POLCO I.1 B.63found calculated found calculated found calculated found calculatedfound calculated 31.25 — 30 — — — — — — 1 30 — — — — — 31.25 1 60 51application rate herbicidal activity against a.i. in g/ha POLCO MATCHALOMY I.1 B.63 found calculated found calculated found calculated foundcalculated found calculated 125 — 80 — 75 — 30 — — — — 0.5 20 — 30 — 0 —— — 125 0.5 100 84 100 83 60 30 application rate herbicidal activityagainst a.i. in g/ha VIOAR I.1 B.63 found calculated found calculatedfound calculated found calculated found calculated 62.5 — 0 — — — — — —0.5 65 — — — — — 62.5 0.5 85 65

Use Example 41

Synergistic herbicidal action of the composition 1.52 applied by thepost emergence method: treatment by the mixture of compound(I.1)+penoxsulam (B.52)

application rate herbicidal activity against a.i. in g/ha VIOAR I.1 B.52found calculated found calculated found calculated found calculated 125— 0 — — — — — 5 60 — — — — 125 5 80 60 application rate herbicidalactivity against a.i. in g/ha ERICA I.1 B.52 found calculated foundcalculated found calculated found calculated found calculated 62.5 — 35— — — — — — 5 90 — — — — — 62.5 5 98 94 application rate herbicidalactivity against a.i. in g/ha ABUTH ERICA I.1 B.52 found calculatedfound calculated found calculated found calculated found calculated31.25 — 15 — 0 — — — — — 5 90 — 90 — — — — 31.25 5 98 92 98 90application rate herbicidal activity against a.i. in g/ha ALOMY VIOARAPESV GERDI I.1 B.52 found calculated found calculated found calculatedfound calculated found calculated 125 — 30 — 0 — 35 — 65 — — — 2.5 55 —0 — 55 — 80 — — 125 2.5 80 69 40 0 75 71 98 93 application rateherbicidal activity against a.i. in g/ha ALOMY APESV VIOAR ABUTH GERDII.1 B.52 found calculated found calculated found calculated foundcalculated found calculated 62.5 — 25 — 20 — 0 — 60 — 65 — — 2.5 55 — 55— 0 — 85 — 80 — 62.5 2.5 80 66 90 64 40 0 98 94 98 93 application rateherbicidal activity against a.i. in g/ha ERICA I.1 B.52 found calculated62.5 — 35 — — 2.5 90 — 62.5 2.5 98 94 application rate herbicidalactivity against a.i. in g/ha ALOMY GERDI ERICA ABUTH I.1 B.52 foundcalculated found calculated found calculated found calculated foundcalculated 31.25 — 25 — 50 — 0 — 15 — — — 2.5 55 — 80 — 90 — 85 — —31.25 2.5 80 66 98 90 98 90 90 87

Use Example 42

Synergistic herbicidal action of the composition 1.88 applied by thepost emergence method: treatment by the mixture of compound(I.1)+flumioxazin (B.88)

application rate herbicidal activity against a.i. in g/ha PAPRH APESVGERDI ALOMY I.1 B.88 found calculated found calculated found calculatedfound calculated 62.5 — 75 — 10 — 0 — 0 — — 2 75 — 65 — 70 — 20 — 62.5 2100 94 75 69 75 70 30 20 application rate herbicidal activity againsta.i. in g/ha PAPRH APESV I.1 B.88 found calculated found calculatedfound calculated found calculated found calculated 31.25 — 75 — 0 — — —— — 2 75 — 65 — — — — 31.25 2 100 94 70 65 application rate herbicidalactivity against a.i. in g/ha PAPRH I.1 B.88 found calculated foundcalculated found calculated found calculated found calculated 15.62 — 70— — — — — — 2 75 — — — — — 15.62 2 100 93 application rate herbicidalactivity against a.i. in g/ha PAPRH GERDI APESV ALOMY KCHSC I.1 B.88found calculated found calculated found calculated found calculatedfound calculated 62.5 — 75 — 0 — 10 — 0 — 80 — — 1 25 — 70 — 25 — 0 — 85— 62.5 1 100 90 70 55 33 40 0 100 97 application rate herbicidalactivity against a.i. in g/ha PAPRH KCHSC APESV ABUTH I.1 B.88 foundcalculated found calculated found calculated found calculated foundcalculated 31.25 — 75 — 55 — 0 — 60 — — — 1 25 — 85 — 25 — 90 — — 31.251 100 85 100 93 45 25 100 96 application rate herbicidal activityagainst a.i. in g/ha KCHSC APESV I.1 B.88 found calculated foundcalculated found calculated found calculated found calculated 15.62 — 45— 0 — — — — — 1 85 — 25 — — — — 15.62 1 100 92 60 25

Use Example 43

Synergistic herbicidal action of the composition 1.95 applied by thepost emergence method: treatment by the mixture of compound(I.1)+trifludimoxazin (B.95)

application rate herbicidal activity against a.i. in g/ha ECHCG GERDIMATCH ERICA GALAP I.1 B.95 found calculated found calculated foundcalculated found calculated found calculated 62.5 — 55 — 0 — 65 — 10 —60 — 2 45 — 65 — 65 — 45 — 75 62.5 2 85 75 100 65 100 88 100 51 95 90application rate herbicidal activity against a.i. in g/ha MATCH ERICAGALAP I.1 B.95 found calculated found calculated found calculated foundcalculated found calculated 31.25 — 10 — 0 — 50 — — — — 2 65 — 45 — 75 —— — 31.25 2 100 69 100 45 95 88 application rate herbicidal activityagainst a.i. in g/ha ERICA I.1 B.95 found calculated found calculatedfound calculated found calculated found calculated 15.62 — 0 — — — — — —2 45 — — — — — 15.62 2 65 45 application rate herbicidal activityagainst a.i. in g/ha ALOMY PAPRH ERICA GERDI APESV I.1 B.95 foundcalculated found calculated found calculated found calculated foundcalculated 62.5 — 0 — 75 — 10 — 0 — 10 — — 1 25 — 35 — 40 — 65 — 30 —62.5 1 60 25 100 84 60 46 75 65 55 37 application rate herbicidalactivity against a.i. in g/ha ALOMY PAPRH MATCH ERICA GALAP I.1 B.95found calculated found calculated found calculated found calculatedfound calculated 31.25 — 0 — 75 — 10 — 0 — 50 — — 1 25 — 35 — 30 — 40 —75 — 31.25 1 55 25 100 84 100 37 55 40 90 85 application rate herbicidalactivity against a.i. in g/ha MATCH ERICA ECHCG APESV I.1 B.95 foundcalculated found calculated found calculated found calculated foundcalculated 15.62 — 10 — 0 — 10 — 0 — — — 1 30 — 40 — 25 — 30 — — 15.62 155 37 55 40 45 33 40 30

Use Example 44

Synergistic herbicidal action of the composition 1.57 applied by thepost emergence method: treatment by the mixture of compound(I.1)+pyroxsulam (B.57)

application rate herbicidal activity against a.i. in g/ha PAPRH ERICAI.1 B.57 found calculated found calculated found calculated foundcalculated 62.5 — 75 — 10 — — — — 2 0 — 75 — — — 62.5 2 90 75 98 78application rate herbicidal activity against a.i. in g/ha IPOHE I.1 B.57found calculated found calculated found calculated found calculatedfound calculated 62.5 — 30 — — — — — — 1 80 — — — — — 62.5 1 98 86

Use Example 45

Synergistic herbicidal action of the composition 1.89 applied by thepost emergence method: treatment by the mixture of compound(I.1)+fomesafen (B.89)

application rate herbicidal activity against a.i. in g/ha GERDI IPOHEERICA I.1 B.89 found calculated found calculated found calculated foundcalculated 62.5 — 0 — 30 — 10 — — — 25 25 — 85 — 20 — — 62.5 25 75 25100 90 35 28 application rate herbicidal activity against a.i. in g/haSTEME IPOHE ABUTH I.1 B.89 found calculated found calculated foundcalculated found calculated found calculated 31.25 — 0 — 25 — 60 — — — —25 0 — 85 — 90 — — — 31.25 25 65 0 100 89 100 96 application rateherbicidal activity against a.i. in g/ha STEME IPOHE GERDI I.1 B.89found calculated found calculated found calculated found calculatedfound calculated 15.62 — 0 — 25 — 0 — — — — 25 0 — 85 — 25 — — — 15.6225 20 0 100 89 35 25 application rate herbicidal activity against a.i.in g/ha ALOMY GERDI VIOAR IPOHE I.1 B.89 found calculated foundcalculated found calculated found calculated found calculated 62.5 — 0 —0 — 25 — 30 — — — 12.5 25 — 25 — 55 — 85 — — 62.5 12.5 45 25 65 25 10066 100 90 application rate herbicidal activity against a.i. in g/haSTEME I.1 B.89 found calculated found calculated found calculated foundcalculated found calculated 31.25 — 0 — — — — — — 12.5 0 — — — — — 31.2512.5 20 0 application rate herbicidal activity against a.i. in g/haPOLCO I.1 B.89 found calculated found calculated found calculated foundcalculated found calculated 15.62 — 0 — — — — — — 12.5 95 — — — — —15.62 12.5 100 95

Use Example 46

Synergistic herbicidal action of the composition 1.167 applied by thepost emergence method: treatment by the mixture of compound(I.1)+quinclorac (B.167)

application rate herbicidal activity against a.i. in g/ha POLCO ABUTHGERDI MATCH I.1 B.167 found calculated found calculated found calculatedfound calculated 62.5 — 40 — 0 — 60 — 0 — — 125 30 — 70 — 0 — 30 — 62.5125 100 58 80 70 100 60 50 30 application rate herbicidal activityagainst a.i. in g/ha ECHCG I.1 B.167 found calculated found calculatedfound calculated found calculated found calculated 31.25 — 10 — — — — —— 125 20 — — — — — 31.25 125 50 28 application rate herbicidal activityagainst a.i. in g/ha POLCO ECHCG I.1 B.167 found calculated foundcalculated found calculated found calculated found calculated 15.62 — 10— 0 — — — — — 125 30 — 20 — — — — 15.62 125 50 37 40 20 application rateherbicidal activity against a.i. in g/ha ABUTH MATCH POLCO KCHSC I.1B.167 found calculated found calculated found calculated foundcalculated found calculated 62.5 — 0 — 0 — 40 — 70 — — — 62.5 65 — 0 — 0— 0 — — 62.5 62.5 75 65 40 0 50 40 80 70 application rate herbicidalactivity against a.i. in g/ha KCHSC I.1 B.167 found calculated foundcalculated found calculated found calculated found calculated 31.25 — 30— — — — — — 62.5 0 — — — — — 31.25 62.5 60 30 application rateherbicidal activity against a.i. in g/ha POLCO I.1 B.167 foundcalculated found calculated found calculated found calculated foundcalculated 15.62 — 10 — — — — — — 62.5 0 — — — — — 15.62 62.5 50 10

Use Example 47

Synergistic herbicidal action of the composition 1.103 applied by thepost emergence method: treatment by the mixture of compound(I.1)+picolinafen (B.103)

application rate herbicidal activity against a.i. in g/ha POLCO GERDIERICA KCHSC I.1 B.103 found calculated found calculated found calculatedfound calculated 62.5 — 40 — 60 — 0 — 70 — — 15 70 — 0 — 65 — 60 — 62.515 100 82 100 60 100 65 100 88 application rate herbicidal activityagainst a.i. in g/ha GERDI PAPRH ERICA IPOHE KCHSC I.1 B.103 foundcalculated found calculated found calculated found calculated foundcalculated 31.25 — 30 — 30 — 0 — 70 — 30 — — 15 0 — 70 — 65 — 60 — 60 —31.25 15 60 60 100 79 100 65 98 88 85 72 application rate herbicidalactivity against a.i. in g/ha STEME PAPRH I.1 B.103 found calculatedfound calculated found calculated found calculated found calculated15.62 — 60 — 30 — — — — — 15 65 — 70 — — — — 15.62 15 100 86 100 79application rate herbicidal activity against a.i. in g/ha POLCO GERDIERICA KCHSC GALAP I.1 B.103 found calculated found calculated foundcalculated found calculated found calculated 62.5 — 40 — 60 — 0 — 70 —50 — — 7.5 40 — 0 — 25 — 60 — 70 — 62.5 7.5 100 64 100 60 40 25 100 8895 85 application rate herbicidal activity against a.i. in g/ha ECHCGGERDI KCHSC I.1 B.103 found calculated found calculated found calculatedfound calculated found calculated 31.25 — 10 — 30 — 30 — — — — 7.5 20 —0 — 60 — — — 31.25 7.5 40 28 100 30 85 72 application rate herbicidalactivity against a.i. in g/ha POLCO GERDI IPOHE I.1 B.103 foundcalculated found calculated found calculated found calculated foundcalculated 15.6 — 10 — 0 — 20 — — — — 7.5 40 — 0 — 40 — — — 15.6 7.5 9846 30 0 65 52

Use Example 48

Synergistic herbicidal action of the composition 1.91 applied by thepost emergence method: treatment by the mixture of compound(I.1)+oxyfluorfen (B.91)

application rate herbicidal activity against a.i. in g/ha ERICA I.1 B.91found calculated found calculated found calculated found calculated 62.5— 0 — — — — — 200 90 — — — — 62.5 200 100 90 application rate herbicidalactivity against a.i. in g/ha ERICA I.1 B.91 found calculated foundcalculated found calculated found calculated found calculated 31.25 — 0— — — — — — 200 90 — — — — — 31.25 200 100 90 application rateherbicidal activity against a.i. in g/ha ECHCG ERICA ALOMY I.1 B.91found calculated found calculated found calculated found calculatedfound calculated 62.5 — 50 — 0 — 0 — — — — 100 60 — 0 — 85 — — — 62.5100 95 80 100 0 98 85 application rate herbicidal activity against a.i.in g/ha ECHCG AMBEL ERICA ALMOY I.1 B.91 found calculated foundcalculated found calculated found calculated found calculated 31.25 — 10— 0 — 0 — 0 — — — 100 60 — 70 — 0 — 85 — — 31.25 100 90 64 98 70 90 0 9585 application rate herbicidal activity against a.i. in g/ha ECHCG AMBELERICA ALMOY I.1 B.91 found calculated found calculated found calculatedfound calculated found calculated 15.62 — 0 — 0 — 0 — 0 — — — 100 60 —70 — 0 — 85 — — 15.62 100 85 60 98 70 65 0 98 85

Use Example 49

Synergistic herbicidal action of the composition 1.144 applied by thepost emergence method: treatment by the mixture of compound(I.1)+aminopyralid (B.144)

application rate herbicidal activity against a.i. in g/ha POLCO I.1B.144 found calculated found calculated found calculated foundcalculated 62.5 — 40 — — — — — 8 98 — — — — 62.5 8 100 99 applicationrate herbicidal activity against a.i. in g/ha AMBEL KCHSC I.1 B.144found calculated found calculated found calculated found calculatedfound calculated 31.25 — 0 — 30 — — — — — 8 75 — 0 — — — — 31.25 8 85 7555 30 application rate herbicidal activity against a.i. in g/ha AMBELKCHSC I.1 B.144 found calculated found calculated found calculated foundcalculated found calculated 15.625 — 0 — 0 — — — — — 8 75 — 0 — — — —15.625 8 85 75 20 0 application rate herbicidal activity against a.i. ing/ha APESV POLCO ABUTH GERDI KCHSC I.1 B.144 found calculated foundcalculated found calculated found calculated found calculated 62.5 — 0 —40 — 0 — 60 — 70 — — 4 0 — 98 — 0 — 30 — 0 — 62.5 4 20 0 100 99 40 0 7060 80 70 application rate herbicidal activity against a.i. in g/ha GERDIVIOLA I.1 B.144 found calculated found calculated found calculated foundcalculated found calculated 15.625 — 0 — 0 — — — — — 4 0 — 0 — — — —15.625 4 20 0 35 0

Use Example 50

Synergistic herbicidal applied by the post emergence method: treatmentby the mixture of compound (I.1)+DMTA

application rate herbicidal activity against a.i. in g/ha GERDI IPOHEI.1 DMTA found calculated found calculated found calculated foundcalculated 125 — 70 — 95 — — — — 350 60 — 25 — — — 125 350 95 88 98 96application rate herbicidal activity against a.i. in g/ha ALOMY POLCOMATCH I.1 DMTA found calculated found calculated found calculated 62.5 —0 — 75 — 60 — — 350 45 — 25 — 30 — 62.5 350 55 45 98 81 100 72application rate herbicidal activity against a.i. in g/ha ALOMY AMBELGERDI MATCH I.1 DMTA found calculated found calculated found calculatedfound calculated found calculated 31.25 — 0 — 10 — 10 — 15 — — — 350 45— 20 — 60 — 30 — — 31.25 350 55 45 65 28 65 64 75 41 application rateherbicidal activity against a.i. in g/ha ALOMY APESV GERDI VIOLA I.1DMTA found calculated found calculated found calculated found calculatedfound calculated 125 — 25 — 0 — 70 — 30 — — — 175 0 — 95 — 30 — 0 — —125 175 40 25 100 95 95 79 80 30 application rate herbicidal activityagainst a.i. in g/ha ALOMY ECHCG VIOLA MATCH ERICA I.1 DMTA foundcalculated found calculated found calculated found calculated foundcalculated 62.5 — 0 — 15 — 20 — 60 — 10 — 175 0 — 90 — 0 — 30 — 15 65.5175 20 0 95 92 30 20 80 72 75 24 application rate herbicidal activityagainst a.i. in g/ha POLCO AMBEL GERDI MATCH ERICA I.1 DMTA foundcalculated found calculated found calculated found calculated foundcalculated 31.25 — 20 — 10 — 10 — 15 — 10 — — 175 0 — 0 — 30 — 30 — 15 —31.25 175 40 20 35 10 55 37 60 41 35 15

Use Example 51

Synergistic herbicidal action of the composition 1.178 applied by thepost emergence method: treatment by the mixture of compound(I.1)+indaziflam (B.178)

application rate herbicidal activity against a.i. in g/ha APESV GALAPGERDI I.1 B.178 found calculated found calculated found calculated foundcalculated 125 — 0 — 65 — 70 — — — 3 40 — 65 — 55 — — 125 3 65 40 100 88100 87 application rate herbicidal activity against a.i. in g/ha ERICAKCHSC I.1 B.178 found calculated found calculated found calculated foundcalculated 62.5 — 10 — 60 — — — — 3 15 — 15 — — — 62.5 3 35 24 85 66application rate herbicidal activity against a.i. in g/ha GERDI MATCHKCHSC I.1 B.178 found calculated found calculated found calculated foundcalculated 31.25 — 10 — 15 — 30 — — — 3 55 — 35 — 15 — — 31.25 3 65 6060 45 45 41 application rate herbicidal activity against a.i. in g/haABUTH GALAP MATCH ERICA I.1 B.178 found calculated found calculatedfound calculated found calculated 62.5 — 55 — 65 — 60 — 10 — — 6 60 — 60— 65 — 60 — 62.5 6 90 82 90 86 100 86 100 64 application rate herbicidalactivity against a.i. in g/ha MATCH ABUTH AMBEL GERDI I.1 B.178 foundcalculated found calculated found calculated found calculated 31.25 — 15— 0 — 10 — 10 — — 6 35 — 60 — 70 — 55 — 31.25 6 60 45 65 60 85 73 60 60

Use Example 52

Synergistic herbicidal action of the composition 1.130 applied by thepost emergence method: treatment by the mixture of compound(I.1)+flufenacet (B.130)

application rate herbicidal activity against a.i. in g/ha ALOMY I.1B.130 found calculated found calculated found calculated foundcalculated 125 — 25 — — — — — 100 65 — — — — 125 100 80 74 applicationrate herbicidal activity against a.i. in g/ha ALOMY MATCH ECHCG I.1B.130 found calculated found calculated found calculated foundcalculated found calculated 62.5 — 0 — 60 — 15 — — — — 100 65 — 20 — 65— — — 62.5 100 85 65 100 68 80 70 application rate herbicidal activityagainst a.i. in g/ha ALOMY POLCO GERDI MATCH I.1 B.130 found calculatedfound calculated found calculated found calculated found calculated31.25 — 0 — 20 — 10 — 15 — — — 100 65 — 10 — 10 — 20 — — 31.25 100 85 6540 28 45 19 55 32 application rate herbicidal activity against a.i. ing/ha GERDI VIOAR I.1 B.130 found calculated found calculated foundcalculated found calculated found calculated 125 — 70 — 30 — — — — — 5010 — 80 — — — — 125 50 90 73 98 86 application rate herbicidal activityagainst a.i. in g/ha MATCH ERICA KCHSC APESV I.1 B.130 found calculatedfound calculated found calculated found calculated found calculated 62.5— 60 — 10 — 60 — 0 — — — 50 0 — 0 — 0 — 85 — — 62.5 50 100 60 35 10 6560 95 85 application rate herbicidal activity against a.i. in g/ha GERDIMATCH IPOHE POLCO ALOMY I.1 B.130 found calculated found calculatedfound calculated found calculated found calculated 31.25 — 10 — 15 — 55— 20 — 0 — — 50 10 — 0 — 60 — 10 — 40 — 31.25 50 25 19 80 15 98 82 60 2875 40

Use Example 53

Synergistic herbicidal action applied by the post emergence method:treatment by the mixture of compound (I.1)+cycloxidim

application rate herbicidal activity against a.i. in g/ha GALAP GERDIAPESV I.1 cycloxidim found calculated found calculated found calculatedfound calculated 125 — 65 — 70 — 0 — — — 5 25 — 20 — 30 — — 125 5 85 74100 76 35 30 application rate herbicidal activity against a.i. in g/haMATCH I.1 cycloxidim found calculated found calculated found calculatedfound calculated found calculated 62.5 — 60 — — — — — — 5 65 — — — — —62.5 5 100 86 application rate herbicidal activity against a.i. in g/haGERDI APESV I.1 cycloxidim found calculated found calculated foundcalculated found calculated found calculated 31.25 — 10 — 0 — — — — — 520 — 30 — — — — 31.25 5 40 28 55 30 application rate herbicidal activityagainst a.i. in g/ha VIOAR GERDI I.1 cycloxidim found calculated foundcalculated found calculated found calculated found calculated 125 — 30 —70 — — — — — 2.5 0 — 0 — — — — 125 2.5 80 30 75 70 application rateherbicidal activity against a.i. in g/ha VIOAR I.1 cycloxidim foundcalculated found calculated found calculated found calculated foundcalculated 62.5 — 20 — — — — — — 2.5 0 — — — — — 62.5 2.5 65 20application rate herbicidal activity against a.i. in g/ha GERDI I.1cycloxidim found calculated found calculated found calculated foundcalculated found calculated 31.25 — 10 — — — — — — 2.5 0 — — — — — 31.252.5 25 10

Use Example 54

Synergistic herbicidal action applied by the post emergence method:treatment by the mixture of compound (I.1)+metsulfuron

application rate herbicidal activity against a.i. in g/ha APESV I.1metsulfuron found calculated found calculated found calculated foundcalculated 62.5 — 0 — — — — — 0.25 30 — — — — 62.5 0.25 40 30application rate herbicidal activity against a.i. in g/ha ECHCG ABUTHI.1 metsulfuron found calculated found calculated found calculated foundcalculated found calculated 31.25 — 0 — 0 — — — — — 0.25 25 — 80 — — — —31.25 0.25 30 25 85 80 application rate herbicidal activity against a.i.in g/ha AMBEL POLCO I.1 metsulfuron found calculated found calculatedfound calculated found calculated found calculated 125 — 65 — 65 — — — —— 0.125 0 — 30 — — — — 125 0.125 100 65 100 76 application rateherbicidal activity against a.i. in g/ha ABUTH I.1 metsulfuron foundcalculated found calculated found calculated found calculated foundcalculated 62.5 — 65 — — — — — — 0.125 20 — — — — — 62.5 0.125 100 72application rate herbicidal activity against a.i. in g/ha ABUTH GALAPECHCG MATCH I.1 metsulfuron found calculated found calculated foundcalculated found calculated found calculated 31.25 — 0 — 50 — 0 — 0 — —— 0.125 20 — 10 — 0 — 0 — — 31.25 0.125 55 20 60 55 30 0 90 0

Use Example 55

Synergistic herbicidal action of the composition 1.93 applied by thepost emergence method: treatment by the mixture of compound(I.1)+sulfentrazone (B.93)

application rate herbicidal activity against a.i. in g/ha AMBEL MATCHPOLCO I.1 B.93 found calculated found calculated found calculated foundcalculated 125 — 65 — 0 — 65 — — — 6 30 — 50 — 85 — — 125 6 100 76 10050 100 95 application rate herbicidal activity against a.i. in g/haPOLCO I.1 B.93 found calculated found calculated found calculated foundcalculated found calculated 62.5 — 65 — — — — — — 3 85 — — — — — 62.5 3100 95 application rate herbicidal activity against a.i. in g/ha POLCOMATCH I.1 B.93 found calculated found calculated found calculated foundcalculated found calculated 31.25 — 0 — 0 — — — — — 3 85 — 50 — — — —31.25 3 100 85 100 50 application rate herbicidal activity against a.i.in g/ha AMBEL MATCH APESV ALOMY I.1 B.93 found calculated foundcalculated found calculated found calculated found calculated 125 — 65 —0 — 0 — 15 — — — 1.5 20 — 0 — 10 — 0 — — 125 1.5 85 72 100 0 40 10 25 15application rate herbicidal activity against a.i. in g/ha GALAP APESVALOMY I.1 B.93 found calculated found calculated found calculated foundcalculated found calculated 62.5 — 80 — 0 — 0 — — — — 1.5 45 — 10 — 0 —— — 62.5 1.5 98 89 30 10 20 0 application rate herbicidal activityagainst a.i. in g/ha PAPRH APESV ALOMY I.1 B.93 found calculated foundcalculated found calculated found calculated found calculated 31.25 — 70— 0 — 0 — — — — 1.5 70 — 10 — 0 — — — 31.25 1.5 100 91 30 10 20 0

Use Example 56

Synergistic herbicidal action of the composition 1.32 applied by thepost emergence method: treatment by the mixture of compound(I.1)+imazapic (B.32)

application rate herbicidal activity against a.i. in g/ha AMBEL MATCHAPESV I.1 B.32 found calculated found calculated found calculated foundcalculated 125 — 65 — 0 — 0 — — — 6 65 — 30 — 80 — — 125 6 100 88 100 3085 80 application rate herbicidal activity against a.i. in g/ha APESVI.1 B.32 found calculated found calculated found calculated foundcalculated found calculated 62.5 — 0 — — — — — — 6 80 — — — — — 62.5 685 80 application rate herbicidal activity against a.i. in g/ha IPOHEABUTH I.1 B.32 found calculated found calculated found calculated foundcalculated found calculated 31.25 — 65 — 0 — — — — — 6 75 — 85 — — — —31.25 6 98 91 98 85 application rate herbicidal activity against a.i. ing/ha AMBEL MATCH I.1 B.32 found calculated found calculated foundcalculated found calculated found calculated 125 — 65 — 0 — — — — — 3 0— 0 — — — — 125 3 100 65 100 0 application rate herbicidal activityagainst a.i. in g/ha ALOMY POLCO I.1 B.32 found calculated foundcalculated found calculated found calculated found calculated 62.5 — 0 —65 — — — — — 3 25 — 85 — — — — 62.5 3 30 25 100 95 application rateherbicidal activity against a.i. in g/ha POLCO ALOMY APESV I.1 B.32found calculated found calculated found calculated found calculatedfound calculated 31.25 — 0 — 0 — 0 — — — — 3 85 — 25 — 65 — — — 31.25 395 85 30 25 70 65

Use Example 57

Synergistic herbicidal action of the composition 1.174 applied by thepost emergence method: treatment by the mixture of compound(I.1)+diflufenzopyr (B.174)

application rate herbicidal activity against a.i. in g/ha MATCH I.1B.174 found calculated found calculated found calculated foundcalculated 125 — 0 — — — — — 40 70 — — — — 125 40 100 70 applicationrate herbicidal activity against a.i. in g/ha STEME VIOAR I.1 B.174found calculated found calculated found calculated found calculatedfound calculated 31.25 — 30 — 0 — — — — — 40 50 — 65 — — — — 31.25 40 8065 75 65 application rate herbicidal activity against a.i. in g/ha MATCHAPESV ALOMY I.1 B.174 found calculated found calculated found calculatedfound calculated found calculated 125 — 0 — 0 — 15 — — — — 20 70 — 0 — 0— — — 125 20 100 70 35 0 40 15 application rate herbicidal activityagainst a.i. in g/ha KCHSC ALOMY I.1 B.174 found calculated foundcalculated found calculated found calculated found calculated 62.5 — 85— 0 — — — — — 20 65 — 0 — — — — 62.5 20 100 95 10 0 application rateherbicidal activity against a.i. in g/ha KCHSC ABUTH POLCO ALOMY I.1B.174 found calculated found calculated found calculated foundcalculated found calculated 31.25 — 70 — 0 — 0 — 0 — — — 20 65 — 85 — 30— 0 — — 31.25 20 95 90 90 85 40 30 10 0

Use Example 58

Synergistic herbicidal action of the composition 1.123 applied by thepost emergence method: treatment by the mixture of compound(I.1)+pendimethalin (B.123)

application rate herbicidal activity against a.i. in g/ha ERICA POLCOI.1 B.123 found calculated found calculated found calculated foundcalculated 125 — 75 — 85 — — — — 1000 60 — 65 — — — 125 1000 100 90 10095 application rate herbicidal activity against a.i. in g/ha ERICA I.1B.123 found calculated found calculated found calculated foundcalculated found calculated 62.5 — 75 — — — — — — 1000 60 — — — — — 62.51000 100 90 application rate herbicidal activity against a.i. in g/haGERDI I.1 B.123 found calculated found calculated found calculated foundcalculated found calculated 31.25 — 65 — — — — — — 1000 75 — — — — —31.25 1000 100 91 application rate herbicidal activity against a.i. ing/ha ERICA I.1 B.123 found calculated found calculated found calculatedfound calculated found calculated 125 — 75 — — — — — — 500 30 — — — — —125 500 100 83 application rate herbicidal activity against a.i. in g/haERICA I.1 B.123 found calculated found calculated found calculated foundcalculated found calculated 62.5 — 75 — — — — — — 500 30 — — — — — 62.5500 100 83 application rate herbicidal activity against a.i. in g/haERICA I.1 B.123 found calculated found calculated found calculated foundcalculated found calculated 31.25 — 70 — — — — — — 500 30 — — — — —31.25 500 100 79

Use Example 59

Synergistic herbicidal action of the composition 1.97 applied by thepost emergence method: treatment by the mixture of compound(I.1)+clomazone (B.97)

application rate herbicidal activity against a.i. in g/ha ALOMY ERICAI.1 B.97 found calculated found calculated found calculated foundcalculated 125 — 65 — 75 — — — — 750 60 — 65 — — — 125 750 95 86 100 97application rate herbicidal activity against a.i. in g/ha ALOMY ERICAI.1 B.97 found calculated found calculated found calculated foundcalculated found calculated 62.5 — 25 — 75 — — — — — 750 60 — 65 — — — —62.5 750 85 70 98 91 application rate herbicidal activity against a.i.in g/ha ERICA IPOHE ALOMY I.1 B.97 found calculated found calculatedfound calculated found calculated found calculated 31.25 — 70 — 40 — 0 —— — — 750 65 — 45 — 60 — — — 31.25 750 98 90 75 67 70 60 applicationrate herbicidal activity against a.i. in g/ha ERICA I.1 B.97 foundcalculated found calculated found calculated found calculated foundcalculated 125 — 75 — — — — — — 375 50 — — — — — 125 375 100 88application rate herbicidal activity against a.i. in g/ha ERICA ALOMYVIOAR I.1 B.97 found calculated found calculated found calculated foundcalculated found calculated 62.5 — 75 — 25 — 30 — — — — 375 50 — 45 — 85— — — 62.5 375 100 88 75 59 98 90 application rate herbicidal activityagainst a.i. in g/ha ALOMY VIOAR I.1 B.97 found calculated foundcalculated found calculated found calculated found calculated 31.25 — 0— 20 — — — — — 375 45 — 85 — — — — 31.25 375 60 45 95 88

Use Example 60

Synergistic herbicidal action applied by the post emergence method:treatment by the mixture of compound (I.1)+halosulfuron methyl

application rate a.i. in g/ha herbicidal activity against halosulfuronECHCG I.1 methyl found calculated found calculated found calculatedfound calculated 62.5 — 45 — — — — — 5 45 — — — — 62.5 5 75 70application rate a.i. in g/ha herbicidal activity against halosulfuronALOMY I.1 methyl found calculated found calculated found calculatedfound calculated found calculated 31.25 — 0 — — — — — — 5 10 — — — — —31.25 5 25 10

Use Example 61

Synergistic herbicidal action of the composition 1.134 applied by thepost emergence method: treatment by the mixture of compound(I.1)+S-metolachlor (B.134)

application rate herbicidal activity against a.i. in g/ha ERICA POLCOI.1 B.134 found calculated found calculated found calculated foundcalculated 125 — 75 — 85 — — — — 500 35 — 60 — — — 125 500 100 84 100 94application rate herbicidal activity against a.i. in g/ha ERICA ALOMYI.1 B.134 found calculated found calculated found calculated foundcalculated found calculated 62.5 — 75 — 25 — — — — — 500 35 — 20 — — — —62.5 500 100 84 50 40 application rate herbicidal activity against a.i.in g/ha ERICA AMBEL GERDI VIOAR KCHSC I.1 B.134 found calculated foundcalculated found calculated found calculated found calculated 31.25 — 70— 75 — 65 — 20 — 80 — — 500 35 — 65 — 30 — 0 — 30 — 31.25 500 100 81 10091 100 76 60 20 100 86 application rate herbicidal activity against a.i.in g/ha ERICA POLCO GALAP VIOAR I.1 B.134 found calculated foundcalculated found calculated found calculated found calculated 125 — 75 —85 — 65 — 60 — — — 250 25 — 35 — 45 — 0 — — 125 250 100 81 98 90 100 8165 60 application rate herbicidal activity against a.i. in g/ha VIOARI.1 B.134 found calculated found calculated found calculated foundcalculated found calculated 62.5 — 30 — — — — — — 250 0 — — — — — 62.5250 35 30 application rate herbicidal activity against a.i. in g/haABUTH AMBEL ALOMY I.1 B.134 found calculated found calculated foundcalculated found calculated found calculated 31.25 — 30 — 75 — 0 — — — —250 40 — 25 — 0 — — — 31.25 250 70 58 90 81 20 0

Use Example 62

Synergistic herbicidal action of the composition 1.1 applied by the postemergence method: treatment by the mixture of compound (I.1)+clethodim(B.1)

application rate herbicidal activity against a.i. in g/ha ABUTH GALAPI.1 B.1 found calculated found calculated found calculated foundcalculated 125 — 60 — 95 — — — — 12 25 — 0 — — — 125 12 98 70 100 95application rate herbicidal activity against a.i. in g/ha ABUTH I.1 B.1found calculated found calculated found calculated found calculatedfound calculated 62.5 — 50 — — — — — — 12 25 — — — — — 62.5 12 80 63application rate herbicidal activity against a.i. in g/ha ABUTH GALAPERICA I.1 B.1 found calculated found calculated found calculated foundcalculated found calculated 31.25 — 25 — 50 — 25 — — — — 12 25 — 0 — 0 —— — 31.25 12 55 44 60 50 30 25 application rate herbicidal activityagainst a.i. in g/ha ABUTH I.1 B.1 found calculated found calculatedfound calculated found calculated found calculated 125 — 60 — — — — — —6 0 — — — — — 125 6 98 60 application rate herbicidal activity againsta.i. in g/ha ABUTH APESV I. B.1 found calculated found calculated foundcalculated found calculated found calculated 62.5 — 50 — 15 — — — — — 60 — 75 — — — — 62.5 6 80 50 90 79 application rate herbicidal activityagainst a.i. in g/ha ABUTH POLCO I.1 B.1 found calculated foundcalculated found calculated found calculated found calculated 31.25 — 25— 65 — — — — — 6 0 — 0 — — — — 31.25 6 45 25 98 65

Use Example 63

Synergistic herbicidal action of the composition 1.140 applied by thepost emergence method: treatment by the mixture of compound (I.1)+2,4-D(B.140)

application rate herbicidal activity against a.i. in g/ha ALMOY ABUTHVIOAR I.1 B.140 found calculated found calculated found calculated foundcalculated 125 — 20 — 60 — 80 — — — 62.5 0 — 85 — 65 — — 125 62.5 50 2098 94 100 93 application rate herbicidal activity against a.i. in g/haALOMY ABUTH GALAP VIOAR I.1 B.140 found calculated found calculatedfound calculated found calculated found calculated 62.5 — 10 — 50 — 90 —0 — — — 62.5 0 — 85 — 0 — 65 — — 62.5 62.5 20 10 98 93 98 90 70 65application rate herbicidal activity against a.i. in g/ha POLCO GALAPVIOAR ERICA I.1 B.140 found calculated found calculated found calculatedfound calculated found calculated 31.25 — 65 — 50 — 0 — 25 — — — 62.5 75— 0 — 65 — 80 — — 31.25 62.5 98 91 65 50 70 65 90 85 application rateherbicidal activity against a.i. in g/ha ALOMY ABUTH I.1 B.140 foundcalculated found calculated found calculated found calculated foundcalculated 125 — 20 — 60 — — — — — 31.25 0 — 35 — — — — 125 31.25 45 2090 74 application rate herbicidal activity against a.i. in g/ha ABUTHGALAP VIOAR I.1 B.140 found calculated found calculated found calculatedfound calculated found calculated 62.5 — 50 — 90 — 0 — — — — 31.25 35 —0 — 60 — — — 62.5 31.25 75 68 95 90 65 60 application rate herbicidalactivity against a.i. in g/ha POLCO GALAP ERICA ABUTH MATCH I.1 B.140found calculated found calculated found calculated found calculatedfound calculated 31.25 — 65 — 50 — 25 — 25 — 25 — — 31.25 65 — 0 — 70 —35 — 0 — 31.25 31.25 100 88 65 50 85 78 55 51 30 25

Use Example 64

Synergistic herbicidal action applied by the post emergence method:treatment by the mixture of compound (I.1)+quizalofop-p-ethyl

application rate a.i. in g/ha herbicidal activity against quizalofop-ABUTH I.1 p-ethyl found calculated found calculated found calculatedfound calculated 125 — 60 — — — — — 15 25 — — — — 125 15 98 70application rate a.i. in g/ha herbicidal activity against quizalofop-VIOAR I.1 p-ethyl found calculated found calculated found calculatedfound calculated found calculated 62.5 — 0 — — — — — — 15 0 — — — — —62.5 15 30 0 application rate a.i. in g/ha herbicidal activity againstquizalofop- PAPRH MATCH ERICA I.1 p-ethyl found calculated foundcalculated found calculated found calculated found calculated 31.25 — 65— 25 — 25 — — — — 15 50 — 0 — 20 — — — 31.25 15 98 83 55 25 55 40application rate a.i. in g/ha herbicidal activity against quizalofop-ABUTH VIOAR I.1 p-ethyl found calculated found calculated foundcalculated found calculated found calculated 125 — 60 — 80 — — — — — 7.515 — 0 — — — — 125 7.5 98 66 98 80 application rate a.i. in g/haherbicidal activity against quizalofop- ABUTH ERICA I.1 p-ethyl foundcalculated found calculated found calculated found calculated foundcalculated 31.25 — 25 — 25 — — — — — 7.5 15 — 0 — — — — 31.25 7.5 45 3630 25

Use Example 65

Synergistic herbicidal action of the composition 1.9 applied by the postemergence method: treatment by the mixture of compound (I.1)+profoxydim(B.9)

application rate herbicidal activity against a.i. in g/ha ABUTH ALOMYI.1 B.9 found calculated found calculated found calculated foundcalculated 125 — 60 — 20 — — — — 12 40 — 25 — — — 125 12 98 76 50 40application rate herbicidal activity against a.i. in g/ha ABUTH I.1 B.9found calculated found calculated found calculated found calculatedfound calculated 62.5 — 50 — — — — — — 12 40 — — — — — 62.5 12 98 70application rate herbicidal activity against a.i. in g/ha APESV POLCOI.1 B.9 found calculated found calculated found calculated foundcalculated found calculated 31.25 — 0 — 65 — — — — — 12 55 — 0 — — — —31.25 12 65 55 70 65 application rate herbicidal activity against a.i.in g/ha ABUTH I.1 B.9 found calculated found calculated found calculatedfound calculated found calculated 125 — 60 — — — — — — 6 0 — — — — — 1256 98 60 application rate herbicidal activity against a.i. in g/ha APESVABUTH I.1 B.9 found calculated found calculated found calculated foundcalculated found calculated 62.5 — 15 — 50 — — — — — 6 15 — 0 — — — —62.5 6 45 28 60 50 application rate herbicidal activity against a.i. ing/ha APESV ABUTH I.1 B.9 found calculated found calculated foundcalculated found calculated found calculated 31.25 — 0 — 25 — — — — — 615 — 0 — — — — 31.25 6 50 15 45 25

Use Example 66

Synergistic herbicidal action applied by the post emergence method:treatment by the mixture of compound (I.1)+thiencarbazone

application rate herbicidal activity against a.i. in g/ha APESV ERICAI.1 thiencarbazone found calculated found calculated found calculatedfound calculated 125 — 15 — 65 — — — — 0.5 25 — 85 — — — 125 0.5 45 36100 95

Use Example 67

Synergistic herbicidal action applied by the post emergence method:treatment by the mixture of compound (I.1)+propaquizafop

application rate herbicidal activity against a.i. in g/ha ALOMY GALAPKCHSC I.1 propaquizafop found calculated found calculated foundcalculated found calculated 125 — 25 — 90 — 95 — — — 10 65 — 10 — 10 — —125 10 100 74 100 91 100 96 application rate herbicidal activity againsta.i. in g/ha ALOMY POLCO ABUTH I.1 propaquizafop found calculated foundcalculated found calculated found calculated found calculated 62.5 — 0 —90 — 85 — — — — 10 65 — 0 — 30 — — — 62.5 10 90 65 98 90 98 90application rate herbicidal activity against a.i. in g/ha ALOMY APESVERICA GALAP KCHSC I.1 propaquizafop found calculated found calculatedfound calculated found calculated found calculated 125 — 25 — 15 — 65 —90 — 95 — — 5 55 — 65 — 0 — 0 — 0 — 125 5 85 66 85 70 100 65 100 90 10095 application rate herbicidal activity against a.i. in g/ha APESV POLCOERICA I.1 propaquizafop found calculated found calculated foundcalculated found calculated found calculated 62.5 — 0 — 90 — 75 — — — —5 65 — 0 — 0 — — — 62.5 5 85 65 98 90 100 75

Use Example 68

Synergistic herbicidal action of the composition 1.169 applied by thepost emergence method: treatment by the mixture of compound(I.1)+quinmerac (B.169)

application rate herbicidal activity against a.i. in g/ha ERICA KCHSCI.1 B.169 found calculated found calculated found calculated foundcalculated 125 — 65 — 95 — — — — 125 75 — 25 — — — 125 125 100 91 100 96application rate herbicidal activity against a.i. in g/ha ERICA KCHSCALOMY APESV I.1 B.169 found calculated found calculated found calculatedfound calculated found calculated 125 — 65 — 95 — 25 — 15 — — — 62.5 65— 10 — 0 — 0 — — 125 62.5 100 88 100 96 35 25 25 15 application rateherbicidal activity against a.i. in g/ha ECHCG I.1 B.169 foundcalculated found calculated found calculated found calculated foundcalculated 62.5 — 60 — — — — — — 62.5 0 — — — — — 62.5 62.5 80 60

Use Example 69

Synergistic herbicidal action applied by the post emergence method:treatment by the mixture of compound (I.1)+aclonifen

application rate herbicidal activity against a.i. in g/ha ERICA ALOMYI.1 aclonifen found calculated found calculated found calculated foundcalculated 125 — 65 — 35 — — — — 1000 0 — 70 — — — 125 1000 100 65 90 81application rate herbicidal activity against a.i. in g/ha ERICA MATCHALOMY I.1 aclonifen found calculated found calculated found calculatedfound calculated found calculated 62.5 — 70 — 30 — 0 — — — — 1000 0 — 0— 70 — — — 62.5 1000 100 70 100 30 80 70 application rate herbicidalactivity against a.i. in g/ha POLCO MATCH I.1 aclonifen found calculatedfound calculated found calculated found calculated found calculated31.25 — 20 — 20 — — — — — 1000 85 — 0 — — — — 31.25 1000 100 88 65 20application rate herbicidal activity against a.i. in g/ha ERICA I.1aclonifen found calculated found calculated found calculated foundcalculated 125 — 65 — — — — — 500 0 — — — — 125 500 100 65 applicationrate herbicidal activity against a.i. in g/ha GERDI MATCH ALOMY I.1aclonifen found calculated found calculated found calculated foundcalculated 62.5 — 55 — 30 — 0 — — — 500 70 — 0 — 60 — — 62.5 500 100 87100 30 70 60 application rate herbicidal activity against a.i. in g/haGERDI MATCH ECHCG POLCO I.1 aclonifen found calculated found calculatedfound calculated found calculated 31.25 — 50 — 20 — 70 — 20 — — 500 70 —0 — 80 — 95 — 31.25 500 100 85 100 20 100 94 100 96 application rateherbicidal activity against a.i. in g/ha ERICA ALOMY ECHCG I.1 aclonifenfound calculated found calculated found calculated found calculated 125— 65 — 35 — 85 — — — 250 0 — 30 — 50 — — 125 250 100 65 70 55 100 93application rate herbicidal activity against a.i. in g/ha GERDI MATCHALOMY ECHCG GALAP I.1 aclonifen found calculated found calculated foundcalculated found calculated found calculated 62.5 — 55 — 30 — 0 — 85 —60 — 250 30 — 0 — 30 — 50 — 80 62.5 250 100 69 100 30 65 30 100 93 98 92application rate herbicidal activity against a.i. in g/ha POLCO GERDIMATCH ALOMY ERICA I.1 aclonifen found calculated found calculated foundcalculated found calculated found calculated 31.25 — 20 — 50 — 20 — 0 —50 — 250 85 — 30 — 0 — 30 — 90 31.25 250 100 88 100 65 100 20 60 30 10095

Use Example 70

Synergistic herbicidal action of the composition 1.135 applied by thepost emergence method: treatment by the mixture of compound(I.1)+pretilachlor (B.135)

application rate herbicidal activity against a.i. in g/ha ERICA I.1B.135 found calculated found calculated found calculated foundcalculated 125 — 65 — — — — — 400 20 — — — — 125 400 100 72 applicationrate herbicidal activity against a.i. in g/ha GERDI MATCH I.1 B.135found calculated found calculated found calculated found calculatedfound calculated 62.5 — 55 — 30 — — — — — 400 0 — 0 — — — — 62.5 400 7055 100 30 application rate herbicidal activity against a.i. in g/haABUTH GERDI MATCH I.1 B.135 found calculated found calculated foundcalculated found calculated found calculated 31.25 — 20 — 50 — 20 — — —— 400 0 — 0 — 0 — — — 31.25 400 40 20 65 50 60 20 application rateherbicidal activity against a.i. in g/ha ERICA I.1 B.135 foundcalculated found calculated found calculated found calculated foundcalculated 125 — 65 — — — — — — 200 0 — — — — — 125 200 100 65application rate herbicidal activity against a.i. in g/ha GALAP GERDIMATCH ERICA I.1 B.135 found calculated found calculated found calculatedfound calculated found calculated 62.5 — 60 — 55 — 30 — 70 — — — 200 0 —0 — 0 — 0 — — 62.5 200 80 60 100 55 100 30 95 70 application rateherbicidal activity against a.i. in g/ha POLCO ABUTH MATCH I.1 B.135found calculated found calculated found calculated found calculatedfound calculated 31.25 — 20 — 20 — 20 — — — — 200 0 — 0 — 0 — — — 31.25200 65 20 50 20 40 20 application rate herbicidal activity against a.i.in g/ha ERICA I.1 B.135 found calculated found calculated foundcalculated found calculated found calculated 125 — 65 — — — — — — 100 0— — — — — 125 100 100 65 application rate herbicidal activity againsta.i. in g/ha GERDI MATCH I.1 B.135 found calculated found calculatedfound calculated found calculated found calculated 62.5 — 55 — 30 — — —— — 100 0 — 0 — — — — 62.5 100 85 55 60 30 application rate herbicidalactivity against a.i. in g/ha ABUTH GERDI MATCH I.1 B.135 foundcalculated found calculated found calculated found calculated foundcalculated 31.25 — 20 — 50 — 20 — — — — 100 0 — 0 — 0 — — — 31.25 100 5020 65 50 40 20

Use Example 71

Synergistic herbicidal action applied by the post emergence method:treatment by the mixture of compound (I.1)+methyl oleate

application rate herbicidal activity against a.i. in g/ha ERICA I.1methyloleate found calculated found calculated found calculated foundcalculated 125 — 65 — — — — — 12 0 — — — — 125 12 100 65 applicationrate herbicidal activity against a.i. in g/ha GERDI MATCH I.1methyloleate found calculated found calculated found calculated foundcalculated found calculated 62.5 — 55 — 30 — — — — — 12 0 — 0 — — — —62.5 12 70 55 100 30 application rate herbicidal activity against a.i.in g/ha POLCO ABUTH GALAP I.1 methyloleate found calculated foundcalculated found calculated found calculated found calculated 31.25 — 20— 20 — 60 — — — — 12 0 — 0 — 0 — — — 31.25 12 40 20 30 20 65 60application rate herbicidal activity against a.i. in g/ha ERICA I.1methyloleate found calculated found calculated found calculated foundcalculated found calculated 125 — 65 — — — — — — 6 0 — — — — — 125 6 9065 application rate herbicidal activity against a.i. in g/ha MATCH GERDII.1 methyloleate found calculated found calculated found calculatedfound calculated found calculated 62.5 — 30 — 55 — — — — — 6 0 — 0 — — —— 62.5 6 100 30 65 55 application rate herbicidal activity against a.i.in g/ha POLCO ABUTH I.1 methyloleate found calculated found calculatedfound calculated found calculated found calculated 31.25 — 20 — 20 — — —— — 6 0 — 0 — — — — 31.25 6 95 20 50 20 application rate herbicidalactivity against a.i. in g/ha ERICA I.1 methyloleate found calculatedfound calculated found calculated found calculated found calculated 125— 65 — — — — — — 3 0 — — — — — 125 3 100 65 application rate herbicidalactivity against a.i. in g/ha GERDI MATCH I.1 methyloleate foundcalculated found calculated found calculated found calculated foundcalculated 62.5 — 55 — 30 — — — — — 3 0 — 0 — — — — 62.5 3 70 55 100 30application rate herbicidal activity against a.i. in g/ha POLCO MATCHI.1 methyloleate found calculated found calculated found calculatedfound calculated found calculated 31.25 — 20 — 20 — — — — — 3 0 — 0 — —— — 31.25 3 70 20 30 20

1. A herbicidal composition comprising as component A) anisoxazolo[5,4-b]pyridine compound of formula I

wherein the variables are as defined below: R¹ is selected from thegroup consisting of hydrogen, halogen, C₁-C₆-alkyl and C₁-C₆-haloalkyl;R² is selected from the group consisting of hydrogen, C₁-C₆-alkyl,C₁-C₆-haloalkyl, C₁-C₆-hydroxyalkyl, C₃-C₆-cycloalkyl,C₃-C₆-halocycloalkyl, C₂-C₆-alkenyl and C₂-C₆-alkynyl; R³ is selectedfrom the group consisting of hydrogen, halogen, hydroxy, C₁-C₆-alkyl,C₁-C₆-haloalkyl, C₁-C₆-hydroxyalkyl, C₁-C₆-alkoxy-C₁-C₆-alkyl,C₁-C₆-haloalkoxy-C₁-C₆-alkyl, C₃-C₆-cycloalkyl-C₁-C₆-alkyl,C₃-C₆-halocycloalkyl-C₁-C₆-alkyl, C₃-C₆-cycloalkyl,C₃-C₆-halocycloalkyl, C₁-C₄-alkyl-C₃-C₆-cycloalkyl, C₃-C₆-cycloalkenyl,C₃-C₆-halocycloalkenyl, phenyl-C₁-C₆-alkyl, heterocyclyl-C₁-C₆-alkyl,C₂-C₆-alkenyl, C₂-C₆-haloalkenyl, C₂-C₆-alkynyl, C₂-C₆-haloalkynyl,C₁-C₆-alkoxy, C₁-C₆-haloalkoxy, C₁-C₆-alkylthio, C₁-C₆-haloalkylthio,amino, C₁-C₆-alkylamino, N,N-di-(C₁-C₆)-alkylamino, heterocyclyl andphenyl; wherein heterocyclyl is a 5- or 6-membered saturated, partiallyunsaturated or aromatic monocyclic ring, which contains 1, 2, 3 or 4heteroatoms selected from the group consisting of O, N and S as ringmembers; and wherein the heterocyclyl and phenyl moieties of R³ can beunsubstituted or substituted with one or more radicals selected from thegroup consisting of halogen, hydroxy, nitro, cyano, C₁-C₄-haloalkyl,C₁-C₄-alkoxy-C₁-C₄-alkyl, C₃-C₆-cycloalkyl, C₂-C₆-alkenyl,C₂-C₆-alkynyl, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy, C₁-C₄-alkoxycarbonyl,C₁-C₄-alkylthio, C₁-C₄-alkylsulfonyl, amino, C₁-C₄-alkylamino,heterocyclyl and phenyl; or its agriculturally acceptable salt,carboxylic ester, thioester or amide; and as component B) at least onefurther herbicide selected from b3) photosynthesis inhibitors.
 2. Thecomposition of claim 1, wherein component A is anisoxazolo[5,4-b]pyridine of formula (I), wherein R¹ is hydrogen, R² iscyclopropyl, R³ is cyclopropyl, methyl or 1,1-dimethylethoxy or anagriculturally useful salt thereof.
 3. The composition of claim 1,wherein the relative amount of the isoxazolo[5,4-b]pyridine compound offormula I to the at least one component B is from 250:1 to 1:250.
 4. Anagrochemical composition comprising the herbicidal composition of claim1, at least one inert liquid and/or solid carrier and, if desired, atleast one further additive.
 5. A method for controlling unwantedvegetation, comprising allowing the composition of claim 1 to act onplants, their seeds and/or their habitat.
 6. The method of claim 5,wherein the unwanted vegetation is controlled in a crop field where cropplants are cultivated.
 7. The method of claim 6, wherein the crop plantsare selected from cereals, corn, soybean, rice, millet, oilseed rape,cotton, sugarcane, potatoes, legumes, turf and permanent crops.
 8. Themethod of claim 7, wherein component A is an isoxazolo[5,4-b]pyridine offormula (I), wherein R¹ is hydrogen, R² is cyclopropyl, R³ iscyclopropyl, methyl or 1,1-dimethylethoxy or an agriculturally usefulsalt thereof.
 9. The method of claim 8, wherein the relative amount ofthe isoxazolo[5,4-b]pyridine compound of formula I to the at least onecomponent B is from 250:1 to 1:250.